# Bioderm, Inc.

- Location (FDA's records): Wheaton, IL
- FDA decisions: 14 (1987–1999): 14 510(k) clearances
- Product codes: KMF (7), MGP (3), FRO (2), NAE (1), EXI (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
- Biomet Merck GmbH: 1 (https://510kreport.com/company/biomet-merck)
- Polymedics Innovations, GmbH: 1 (https://510kreport.com/company/polymedics-innovations)

## Its most-cited devices
- K982939: BTF Thin Film Wound Dressing (1998), cited by 2

## Recent decisions
- K990955: Modification of:Bioderm Foam Wound Dressing (May 18, 1999)
- K982778: Bioderm Foam Wound Dressing (Oct 21, 1998)
- K982939: BTF Thin Film Wound Dressing (Oct 13, 1998)
- K980451: Bioderm Calcium Alginate Dressing (Apr 9, 1998)
- K973429: Bioderm Foam Wound Dressing (Dec 1, 1997)
- K963950: Bioderm Eid Male External Incontinence Device (Jan 10, 1997)
- K963602: Bioderm PVP Foam Wound Dressing (Oct 30, 1996)
- K951166: Bioderm Medical Hydrogel Island Dressing (Jun 21, 1995)

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