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FDA PMA

Implant, dermal, for aesthetic use

PMA Number: P050037 · 2026-06-26

ApplicantMerz North America, Inc.
Decision Date2026-06-26
PMA NumberP050037
Product CodeLMH
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeSU

Device Summary

Implant, dermal, for aesthetic use is the device name listed in this FDA 510(k) record. The listed applicant is Merz North America, Inc.. It received FDA 510(k) clearance on 2026-06-26. The device is classified under product code LMH. It was reviewed by the SU advisory panel.

Frequently Asked Questions

What is the Implant, dermal, for aesthetic use?

Implant, dermal, for aesthetic use is a medical device that received FDA 510(k) clearance on 2026-06-26. The listed applicant is Merz North America, Inc..

When did Implant, dermal, for aesthetic use receive FDA 510(k) clearance?

The clearance date for Implant, dermal, for aesthetic use can be found in the official FDA records.

Who is the listed applicant for Implant, dermal, for aesthetic use?

The FDA 510(k) record lists Merz North America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Implant, dermal, for aesthetic use?

The FDA product code for Implant, dermal, for aesthetic use is LMH.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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