# Cutting Edge Technologies, Inc.

- Location (FDA's records): West Chester, PA
- FDA decisions: 2 (1995–1997): 2 510(k) clearances
- Product codes: FMI (1), KGX (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
- K963595: Seragard Vascular Access Device (Jan 6, 1997)
- K952606: Targett Patch (Dec 21, 1995)

Source page: https://510kreport.com/company/cutting-edge-technologies