Biocomposites, Ltd.
Biocomposites, Ltd. holds FDA 510(k) medical device clearances, first cleared 2000, most recent 2026, with 1 FDA device recall on record.
Top product codes for Biocomposites, Ltd.
FDA recalls by Biocomposites, Ltd.
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 Biocomposites, Ltd.
- K251680 — Biosteon® Screw
- K242865 — Synicem Hip Spacer; Synicem Knee Spacer; Synicem Shoulder Spacer
- K250521 — NanoBone® SBX Putty; NanoBone® QD
- K212721 — Genex Bone Graft Substitute
- K141830 — STIMULAN KIT, STIMULAN RAPID CURE
- K082381 — GENEX
- K082383 — FORTOSS VITAL
- K073341 — GENEX PUTTY
- K081428 — MODIFICATION TO DOUBLEPLAY SUTURE ANCHOR
- K072127 — DOMINATOR
- K071952 — GRAFTLOCK SCREW, ST SCREW
- K071091 — MODIFICATION TO BILOK SCREW
- K071115 — MODIFICATION TO BILOK ST SCREW
- K061949 — DOUBLEPLAY SUTURE ANCHOR
- K061311 — ALLOGRAN-R
- K050170 — FORTOSS VITAL BONE GRAFT SUBSTITUTE
- K043514 — ALLOGRAN-N-BONE VOID FILLER
- K040265 — LITTLE GRAFTER SCREW
- K040600 — GENEX BONE GRAFT SUBSTITUTE
- K033792 — BILOK ST SCREW
- K021551 — STIMULAN - CALCIUM SULFATE BONE VOID FILLER KIT
- K021351 — BIOSTEON CROSS PIN
- K003954 — STIMULAN - CALCIUM SULFATE BONE VOID FILLER KIT
- K003641 — BIOLOK SCREW, BIOSTEON SCREW
- K002070 — BIOLOK SCREW
- K001724 — STIMULAN -CALCIUM SULFATE BONE VOID FILTER
- K993238 — FORTOSS-CEMA
Data sourced from openFDA. This site is unofficial and independent of the FDA.