# Bioaccess, Inc.

- Location (FDA's records): Silver Spring, MD
- FDA decisions: 3 (1995–1997): 3 510(k) clearances
- Product codes: GDM (2), KNW (1)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 2 (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
- Popper & Sons, Inc.: 1 (https://510kreport.com/company/popper-sons)
- Zimmer, Inc.: 1 (https://510kreport.com/company/zimmer)

## Firms that cite its devices most
- Vidacare Corporation: 1 (https://510kreport.com/company/vidacare)

## Its most-cited devices
- K953064: Bioaccess Marrow Harvest System (1995), cited by 2

## Recent decisions
- K971114: Bioaccess Marrow Harvest System (Jun 3, 1997)
- K954151: Bioaccess Bone Biopsy System (Sep 15, 1995)
- K953064: Bioaccess Marrow Harvest System (Aug 7, 1995)

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