Biologic Therapies, Inc.
Biologic Therapies, Inc. holds FDA 510(k) medical device clearance, cleared in 2015, with 3 FDA device recalls on record.
Top product codes for Biologic Therapies, Inc.
FDA recalls by Biologic Therapies, Inc.
- Z-1374-2015 — Bio-CORE Cannula (Needle) Set
- Z-1372-2015 — Bio-PLASTY Cannula (Needle)
- Z-1373-2015 — Bio-MAC Cannula (Needle) Set
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Biologic Therapies, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.