# Acuderm, Inc.

- Location (FDA's records): Ft. Lauderdale, FL
- FDA decisions: 13 (1983–1994): 13 510(k) clearances
- Product codes: JSJ (3), MDM (2), FMI (1), LRO (1), FZS (1), GEX (1), FYD (1), FMF (1), LRY (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
- K933516: Acu-E Punch (Mar 24, 1994)
- K933265: Acu-Dispo-CE (TM) (Mar 7, 1994)
- K933137: Acu-Suture Kit (Feb 22, 1994)
- K930043: Acu-Evac (Feb 9, 1994)
- K933866: Acu-Hemostatic Ring (Dec 1, 1993)
- K915000: Acu-Guard (Jan 27, 1992)
- K891334: Acu-Curette (Apr 11, 1989)
- K874024: Acu-Micro-Needle (Nov 23, 1987)

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