What Morpheus8 consumables are

Morpheus8 consumables fall into three regulatory categories listed in AccessGUDID under InMode Ltd.: nine single-use tip variants (gamma-sterilized, lot-tracked, GMDN 45048), five reusable applicators (serial-tracked, GMDN 58455), and three multi-modality platforms that carry Morpheus8 applicators (serial-tracked, GMDN 45220). All sit under FDA Class II classification with Product Code GEI and regulation 21 CFR 878.4400. For the underlying device technology and clearance background, see the Morpheus8 device overview. Tip selection drives the per-session consumable cost; applicator selection drives compatibility across generations. The matrix is wider than for most RF microneedling brands in the same category, which is one reason procurement requires a clear mapping of tip to applicator.

The Morpheus8 tip families: a procurement-grade matrix

Across the FDA 510(k) clearances and the AccessGUDID device records, nine Morpheus8 tip variants are currently listed under InMode Ltd. Five are tied directly to a 510(k) clearance summary (the 12, 24, 40, T, and 90 pin configurations). Four others appear in the AccessGUDID record search for Morpheus8 with K-number references, but the specific intended-use language for those submissions was not reviewed in the primary source for this article. The status column in the table below makes that distinction visible per tip.

Burst and Burst Deep applicators: a separate sub-family

The Morpheus8 Burst Applicator (catalog AG613055A, UDI-DI 07290019863120) and the Morpheus8 Burst Deep Applicator (catalog AG613056A, UDI-DI 07290019863137) are listed in AccessGUDID as separate reusable applicators rather than as tip variants. Both belong to the gen-2 catalog series (AG6130xx). The Burst sub-family is marketed as a multi-tier energy delivery design, with each tip insertion intended to support multiple discrete RF pulses at different depths within the same channel.

GUDID submissions for the Morpheus8 Burst Applicator reference K221571, K231790, K251254, and K251632; clearance language for those submissions was not reviewed in primary source for this article. The Burst Deep Applicator is listed under InMode Ltd. in GUDID, but its predicate and indications were not separately verified here. Clinics planning to introduce Burst or Burst Deep into their protocol should read the relevant 510(k) summaries and the manufacturer's instructions for use directly.

Practical procurement note: Burst applicators do not interchange with the original Morpheus8 Applicator or the Morpheus8 Body (Blue), which belong to the gen-1 catalog series. The tip cartridge populations differ as a result, and ordering against the wrong applicator series is the most common avoidable mismatch. The Burst Deep variant in particular is positioned for body work; the body applicators and depth article covers its role alongside Body (Blue) and 90 Applicator.

The Resurfacing tip and the gen-1 body tip family

The Morpheus8 Resurfacing Tip (AG613051A, 24-pin, gen-2 catalog series) is a fractional finishing configuration for surface-layer work, separate from the 24-pin standard tip cleared in K192695. The intended-use language for the resurfacing variant was not reviewed in the primary source for this article, so the catalog entry sits in the GUDID-listed group in the matrix above rather than in the directly cited group.

Two gen-1 body tips remain in active listing. The Morpheus8 Body 40-pin Tip (AG609135A, UDI-DI 07290016633627) was the original deeper-coverage tip for the gen-1 Morpheus8 Applicator and the Body (Blue) applicator. The Morpheus8 3D 40p Tip (AG609135A_3D variant, UDI-DI 17290016633624) is a related gen-1 body configuration. A legacy tip (AG607563A) predates the formal Morpheus8 catalog numbering scheme and appears in older equipment.

Gen-1 vs. Gen-2: how catalog numbering signals compatibility

InMode's Morpheus8 catalog numbering carries useful generational information that procurement teams can read directly. Catalog prefixes in the AG6074xx and AG6091xx ranges belong to the first applicator generation. Prefixes in the AG6130xx and AG6131xx ranges belong to the second generation, which introduced Burst, Burst Deep, and the 90 Applicator alongside the gen-2 tip families. The table below shows the most common pairings as signaled by the numbering pattern.

Compatibility is based on industry-standard usage and clinical experience. The only mapping confirmed in GUDID record-level descriptions is the Morpheus8 90 Tip to the Morpheus8 90 Applicator. Other tip-to-applicator pairings are signaled by the catalog numbering pattern but were not stated in primary source for this article; verification against the specific applicator and its instructions for use is the buying clinic's responsibility.

For compatibility deep-dives in adjacent RF microneedling brands, see the Sylfirm X tips compatibility and Scarlet SRF tips compatibility articles in the same series. For how Morpheus8 sits in the broader landscape of bipolar RF microneedling, ultrasound, mechanical microneedling, monopolar RF, and ablative laser, the Morpheus8 comparison hub walks through each category.

How Morpheus8 consumables are structured: sterilization and tracking

The regulatory grouping under AccessGUDID separates the three categories of consumables by GMDN code: tips carry GMDN 45048 (RF skin contouring system applicator tip), applicators carry 58455 (RF skin surface treatment system applicator), and platforms carry 45220 (multi-modality skin surface treatment system). All carry FDA Product Code GEI and are classified as Class II under 21 CFR 878.4400.

The tracking pattern is consistent across the catalog. Tips are lot-tracked, which is the appropriate tracking unit for disposable batches and supports recall to a specific manufacturing lot. Applicators and platforms are serial-tracked, which identifies the specific hardware unit across its service life. Sterilization is recorded per category: tips ship gamma-sterilized as recorded in the K192695 Summary; applicators and platforms list "Sterilization Prior To Use: No" in their GUDID entries, consistent with reusable hardware. For category context across modalities, see the broader RF microneedling tips and cartridges catalog.

Replacement cycle and procurement planning

Morpheus8 tips are designed for single use, per the GMDN 45048 definition and the K192695 Summary's gamma-sterilization specification. The exact number of treatments per tip, the number of tips typically used per session, and the per-area pass counts are protocol decisions documented in the manufacturer's instructions for use rather than in AccessGUDID; the GUDID record set does not include either treatments per tip or unit-of-use information, so the manufacturer documentation is the authoritative source.

Packaging size is also not recorded in the GUDID listing. Clinics planning procurement against expected case volume usually estimate consumable cost in two layers: a per-tip cost at the catalog level, and an expected tips-per-session figure tied to the specific protocols the clinic runs. The per-session figure varies with tip configuration and treated area. Cost per case is therefore a function of the protocol, not a fixed property of the tip itself. The Morpheus8 cost framework for clinics structures this into the broader machine + consumables + operational decomposition.

Used and refurbished Morpheus8 platforms: what to verify

Clinics evaluating used or refurbished Morpheus8 platforms can verify several items against the public GUDID record before purchase. The platform's catalog number and serial should appear in the AccessGUDID listing under InMode Ltd. (InMode system AG606666A, Envision System AG609993A, or EmPowerRF AG609933A). FDA 510(k) status against the listed product codes is visible in the same record. Configuration matters too, because modified or unlabeled equipment falls outside the cleared envelope and was specifically called out in the FDA's 2025 safety communication on RF microneedling. This article keeps the buyer-side checklist short; the device and equipment article in this series goes into platform selection, marketplace risks, and vendor verification in more depth.

Professionally sourced Morpheus8 tips: how Pinova carries them

Pinova carries professionally sourced Morpheus8 tips for clinics that run InMode Morpheus8 platforms. Inventory covers the active tip configurations across both gen-1 and gen-2 applicator families, with catalog numbering and UDI-DI references visible per SKU. Verification against the specific applicator, platform, and generation in use is the responsibility of the buying clinic. Browse the InMode Morpheus8 Tips collection for current SKUs, pin counts, and packaging.

Frequently asked questions

What is the Morpheus8 Burst applicator?

The Morpheus8 Burst Applicator is a gen-2 reusable applicator listed in AccessGUDID under InMode Ltd. (catalog AG613055A, UDI-DI 07290019863120). It is marketed as a multi-tier RF delivery applicator, designed to dispense radiofrequency at multiple depths within the same tip insertion. The Burst Deep variant (AG613056A) extends that approach for deeper-tissue contexts. Both belong to the gen-2 catalog series and use gen-2 tip families.

What is the difference between Morpheus8 and Morpheus8 Burst?

The original Morpheus8 Applicator (catalog AG607401A, gen-1) delivers RF in a single discrete pulse pattern per tip insertion. The Burst Applicator (AG613055A, gen-2) is marketed as a multi-tier RF delivery applicator that supports multiple discrete RF pulses at different depths within one insertion. Both are reusable applicators that take single-use Morpheus8 tips, but the tip families differ by generation; gen-1 and gen-2 tips do not interchange across applicator generations.

Which Morpheus8 tip fits which applicator?

The only tip-to-applicator pairing confirmed in GUDID record descriptions is the Morpheus8 90 Tip to the Morpheus8 90 Applicator. Other pairings are signaled by InMode's catalog numbering pattern: AG6091xx tips align with gen-1 applicators, and AG6130xx tips align with gen-2 applicators, including Burst. The table in section 5 shows the likely pairings; verification against the specific applicator and the manufacturer's instructions for use is the buying clinic's responsibility.

Are Morpheus8 tips single-use?

Yes. Morpheus8 tips are classified in AccessGUDID under GMDN 45048 (RF skin contouring system applicator tip) and listed as single-use disposables, gamma-sterilized as recorded in the K192695 Summary. The applicators that carry the tips are reusable and serial-tracked; the platforms are likewise reusable and serial-tracked.