# Biodermis Corp.

- Location (FDA's records): Las Vegas, NV
- FDA decisions: 5 (1994–2001): 5 510(k) clearances
- Product codes: MDA (4), GEH (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Neodyne Biosciences, Inc.: 1 (https://510kreport.com/company/neodyne-biosciences)
- Coreleader Biotech Co., Ltd.: 1 (https://510kreport.com/company/coreleader-biotech)

## Its most-cited devices
- K003948: Epi-Derm Silicone Gel Sheeting (2001), cited by 2

## Recent decisions
- K003948: Epi-Derm Silicone Gel Sheeting (Jan 29, 2001)
- K992146: Scaraid Silicone Gel Sheeting (Jul 30, 1999)
- K991604: Epi-Foam Silicone Sheeting (Jun 9, 1999)
- K964047: Cryosil Silicone Gel Sheeting (Mar 19, 1997)
- K942156: Epi-Derm Silicone Gel Sheeting (Jun 13, 1994)

Source page: https://510kreport.com/company/biodermis