# MDD · Device, Dermal Replacement

_ ·  · Class 3_

**Canonical URL:** https://fda-staging.innolitics.com/productcode/MDD

## Overview

- **Product Code:** MDD
- **Device Name:** Device, Dermal Replacement
- **Regulation:** 21 CFR N/A
- **Device Class:** 3
- **Review Panel:** [](/submissions/)
- **Implant:** yes

## Recent Cleared Devices (2 of 2)

| Record | Device Name | Applicant | Decision Date | Decision |
| --- | --- | --- | --- | --- |
| [P900033S042](/device/P900033S042.md) | INTEGRA(R) DERMAL REGENERATION TEMPLATE,INTEGRA(R) MESHED DERMAL REGENERATION TEMPLATE,OMNIGRAFT (TM) DERMAL REGENERATIO | Integra Lifesciences Corp. | Jan 7, 2016 | APPR |
| [P900033S008](/device/P900033S008.md) | INTEGRA DERMAL REGENERATION TEMPLATE | Integra Lifesciences Corp. | Apr 19, 2002 | APPR |

## Top Applicants

- Integra Lifesciences Corp. — 2 clearances

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**Source:** [https://fda-staging.innolitics.com/productcode/MDD](https://fda-staging.innolitics.com/productcode/MDD)

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