Bioretec, Ltd.
Bioretec, Ltd. holds FDA 510(k) medical device clearances, first cleared 2006, most recent 2026.
Top product codes for Bioretec, Ltd.
Recent clearances by Bioretec, Ltd.
- K261057 — ActivaScrew Cannulated COM
- DEN220030 — RemeOs Screw LAG Solid
- K133950 — ACTIVAPIN HT, FUSE LINK (PRIVATE LABLED FOR FOOTMIND, INC.)
- K130716 — BIORETEC ACTIVASCREW INTERFERENCE
- K080879 — ACTIVATM PRODUCT GROUP INCLUDING BIOABSORBABLE DEVICES ACTIVAPIN FUSION, ACTIVANAILTM CONICALTM
- K081392 — BIORETEC ACTIVASCREW, ACTIVASCREW CANNULATED AND ACTIVASCREW CANNULATED WITH ACTIVAPIN
- K072848 — ACTIVASCREW
- K071863 — ACTIVAPIN, NEXFIX RFS PIN, NEXFIX RESORBABLE FIXATION SYSTEM (RFS)
- K062980 — ACTIVASCREW
- K061164 — ACTIVAPIN
Data sourced from openFDA. This site is unofficial and independent of the FDA.