# Carapace, Inc.

- Location (FDA's records): Broken Arrow, OK
- FDA decisions: 22 (1979–1994): 22 510(k) clearances
- Product codes: LRO (6), LGF (2), KKX (1), IRO (1), ITG (1), GDY (1), CAZ (1), LGH (1), MLT (1), MLS (1), FOZ (1), DQO (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
- K931722: Carapace Labor and Delivery Sets (Mar 23, 1994)
- K931822: Carapace Pelvic Exam Trays (Mar 7, 1994)
- K931729: I.V. Start Kit (Feb 22, 1994)
- K931820: Carapace Stillwater Bowl Set (Feb 7, 1994)
- K931669: Carapace Debridement Kits (Feb 7, 1994)
- K931760: Carapace Packing Gauze Trays (Feb 4, 1994)
- K932653: Swisstek 2000(TM) Cast Removal System (Jan 28, 1994)
- K931819: Carapace Suture Removal Trays (Jan 26, 1994)

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