# Bio-Lok Intl., Inc.

- Location (FDA's records): Stillwater, MN
- FDA decisions: 3 (2004–2006): 3 510(k) clearances
- Product codes: DZE (2), LYC (1)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Orthogen, LLC: 1 (https://510kreport.com/company/orthogen)
- Lifecore Biomedical, Inc.: 1 (https://510kreport.com/company/lifecore-biomedical)
- Osteobiologics, Inc.: 1 (https://510kreport.com/company/osteobiologics)
- Atrix Laboratories, Inc.: 1 (https://510kreport.com/company/atrix-laboratories)

## Firms that cite its devices most
- Orthogen, LLC: 1 (https://510kreport.com/company/orthogen)
- Sudimplant SA: 1 (https://510kreport.com/company/sudimplant)

## Its most-cited devices
- K032454: Silhouette (TM) IC or Silhouette (TM) & Laser-Lok (TM) (2004), cited by 2
- K060285: Bonegen - TR (2006), cited by 1

## Recent decisions
- K060285: Bonegen - TR (Mar 16, 2006)
- K041136: Modification to Silhouette IC or Silhouette; Laser-Lok Surface Treatment -Optional Surface Modification to Implants (Oct 22, 2004)
- K032454: Silhouette (TM) IC or Silhouette (TM) & Laser-Lok (TM) (Mar 4, 2004)

Source page: https://510kreport.com/company/bio-lok-intl