# American Biomaterials Corp.

- Location (FDA's records): The Woodlands, TX
- FDA decisions: 6 (1985–1994): 6 510(k) clearances
- Product codes: DQO (1), LRS (1), FOZ (1), LYC (1), MDM (1), ETA (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
- K922455: Evert-O-Cath Catheter (Jul 7, 1994)
- K924725: American Biomed, Inc. Microsurgical Instruments (Feb 5, 1993)
- K915824: Hole Punch (Jan 29, 1993)
- K880371: Bioglass Dental Endosseous Ridge Maintainer (Nov 18, 1988)
- K863796: Creative Care Systems' IV Start Kit (Nov 28, 1986)
- K843461: Bioglass Ossicular Reconstruction Prosth (Jan 9, 1985)

Source page: https://510kreport.com/company/american-biomaterials