# Applied Biomaterial Technologies

- Location (FDA's records): Silverdale, WA
- FDA decisions: 7 (1990–1995): 7 510(k) clearances
- Product codes: FWP (2), MIB (2), MIC (1), LZK (1), FZE (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K945552: Duralastic Sheeting (Jan 31, 1995)
- K935571: Duralastic Sheeting (Jan 31, 1995)
- K931500: The Permaridge Matrix Chin (Nov 17, 1994)
- K913768: Pec Implant (Feb 3, 1992)
- K902284: Zymalar Implant (Sep 12, 1990)
- K902285: The Magnum Chin Implant (Sep 12, 1990)
- K902283: The Nautilus Nasal Implant (Aug 14, 1990)

Source page: https://510kreport.com/company/applied-biomaterial-technologies