# Anchor Implants, Ltd.

- Location (FDA's records): Canada, CA
- FDA decisions: 2 (1987–1988): 2 510(k) clearances
- Product codes: DZE (2)
- 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
- K873939: Adi/B/*/HA-2 Stage Osseo. Hydro. Dental Implant (Mar 15, 1988)
- K871887: Anchor Iia/2 Stage Osseo. Tit. 6/4 Alloy Implant (Jul 31, 1987)

Source page: https://510kreport.com/company/anchor-implants