Biocomposites, Ltd.

27 FDA 510(k) medical device clearances.

Top product codes for Biocomposites, Ltd.

Recent clearances by Biocomposites, Ltd.

K251680 — Biosteon® Screw MAI · 2026-02-17
K242865 — Synicem Hip Spacer; Synicem Knee Spacer; Synicem Shoulder Spacer KWL · 2025-06-12
K250521 — NanoBone® SBX Putty ; NanoBone® QD MQV · 2025-04-07
K212721 — Genex Bone Graft Substitute MQV · 2022-02-04
K141830 — STIMULAN KIT, STIMULAN RAPID CURE MQV · 2015-01-23
K082381 — GENEX MQV · 2008-11-14
K082383 — FORTOSS VITAL LYC · 2008-09-05
K073341 — GENEX PUTTY MQV · 2008-07-09
K081428 — MODIFICATION TO DOUBLEPLAY SUTURE ANCHOR HWC · 2008-06-20
K072127 — DOMINATOR HWC · 2007-08-31
K071952 — GRAFTLOCK SCREW, ST SCREW HWC · 2007-08-14
K071091 — MODIFICATION TO BILOK SCREW HWC · 2007-05-17
K071115 — MODIFICATION TO BILOK ST SCREW HWC · 2007-05-17
K061949 — DOUBLEPLAY SUTURE ANCHOR HWC · 2006-09-25
K061311 — ALLOGRAN-R MQV · 2006-09-22
K050170 — FORTOSS VITAL BONE GRAFT SUBSTITUTE LYC · 2005-08-26
K043514 — ALLOGRAN-N-BONE VOID FILLER MQV · 2005-01-21
K040265 — LITTLE GRAFTER SCREW HWC · 2004-05-28
K040600 — GENEX BONE GRAFT SUBSTITUTE MQV · 2004-05-07
K033792 — BILOK ST SCREW HWC · 2004-03-01
K021551 — STIMULAN - CALCIUM SULFATE BONE VOID FILLER KIT MQV · 2002-11-01
K021351 — BIOSTEON CROSS PIN HWC · 2002-10-17
K003954 — STIMULAN - CALCIUM SULFATE BONE VOID FILLER KIT MQV · 2001-07-12
K003641 — BIOLOK SCREW, BIOSTEON SCREW HWC · 2001-02-08
K002070 — BIOLOK SCREW HWC · 2000-08-25
K001724 — STIMULAN -CALCIUM SULFATE BONE VOID FILTER MQV · 2000-08-04
K993238 — FORTOSS-CEMA LYC · 2000-01-14

Data sourced from openFDA. This site is unofficial and independent of the FDA.