Biopro, Inc.
Biopro, Inc. holds FDA 510(k) medical device clearances, first cleared 1987, most recent 2017, with 37 FDA device recalls on record.
Top product codes for Biopro, Inc.
FDA recalls by Biopro, Inc.
10 most recent of 37- Z-0148-2026 — BioPro Femoral Head (Metal 22, 28, 32, 36, 40) cobalt chromium and ceramic heads Part ID/Description: 18593 HEAD FEMORAL 22MM -3 18594 HEAD FEMORAL 22MM +0 19003 HEAD FEMORAL 28MM-6 19004 HEAD FEMORAL 28MM-3 19005 HEAD FEMORAL 28MM+0 19006 HEAD FEMORAL 28MM+3 19007 HEAD FEMORAL 28MM+6 19008 HEAD FEMORAL 28MM+9 19053 HEAD FEMORAL 36MM -3 19054 HEAD FEMORAL 36MM +0 19055 HEAD FEMORAL 36MM +3 19056 HEAD FEMORAL 36MM +6 19057 HEAD FEMORAL 36MM +9 19130 HEAD FEMORAL 32MM-6 19131 HEAD FEMORAL 32MM-3 19132 HEAD FEMORAL 32MM+0 19133 HEAD FEMORAL 32MM +3 19134 HEAD FEMORAL 32MM+6 19135 HEAD FEMORAL 32MM +9
- Z-0152-2026 — BioPro Endo Head (Ceramic) Product ID/Description 13006 ENDO MODULAR CERAMIC SH 38 13012 ENDO MODULAR CERAMIC SH 51 13013 ENDO MODULAR CERAMIC MD 38 13019 ENDO MODULAR CERAMIC MD 51 13007 ENDO MODULAR CERAMIC SH 41 13008 ENDO MODULAR CERAMIC SH 43 13009 ENDO MODULAR CERAMIC SH 45 13010 ENDO MODULAR CERAMIC SH 47 13011 ENDO MODULAR CERAMIC SH 49 13014 ENDO MODULAR CERAMIC MD 41 13015 ENDO MODULAR CERAMIC MD 43 13016 ENDO MODULAR CERAMIC MD 45 13017 ENDO MODULAR CERAMIC MD 47 13018 ENDO MODULAR CERAMIC MD 49 14823 ENDO MODULAR CERAMIC SH 53 14824 ENDO MODULAR CERAMIC MD 53 14825 ENDO MODULAR CERAMIC SH 55 14826 ENDO MODULAR CERAMIC MD 55 17295 ENDO MODULAR CERAMIC SH 36 17296 ENDO MODULAR CERAMIC MD 36
- Z-0150-2026 — BioPro Bipolar Head Product ID/Description 18130 BIPOLAR HEAD 38MM 18131 BIPOLAR HEAD 39MM 18132 BIPOLAR HEAD 40MM 18133 BIPOLAR HEAD 41MM 18134 BIPOLAR HEAD 42MM 18135 BIPOLAR HEAD 43MM 18136 BIPOLAR HEAD 44MM 18137 BIPOLAR HEAD 45MM 18138 BIPOLAR HEAD 46MM 18139 BIPOLAR HEAD 47MM 18140 BIPOLAR HEAD 48MM 18141 BIPOLAR HEAD 49MM 18142 BIPOLAR HEAD 50MM 18143 BIPOLAR HEAD 51MM 18144 BIPOLAR HEAD 52MM 18145 BIPOLAR HEAD 53MM 18146 BIPOLAR HEAD 54MM 18147 BIPOLAR HEAD 55MM 18148 BIPOLAR HEAD 56MM 18149 BIPOLAR HEAD 57MM 18150 BIPOLAR HEAD 58MM 18151 BIPOLAR HEAD 59MM 18152 BIPOLAR HEAD 60MM
- Z-0149-2026 — BioPro Endo Head (Metal uni-polar, 38-55) Product Number/Description 10179 ENDO MD 38 10180 ENDO MD 41 10181 ENDO MD 43 10182 ENDO MD 45 10183 ENDO MD 47 10184 ENDO MD 49 10185 ENDO MD 51 10186 ENDO MD 53 10187 ENDO MD 55 10188 ENDO SH 38 10189 ENDO SH 41 10190 ENDO SH 43 10191 ENDO SH 45 10192 ENDO SH 47 10193 ENDO SH 49 10194 ENDO SH 51 10195 ENDO SH 53 10196 ENDO SH 55
- Z-0153-2026 — BioPro Femoral Head Product ID/Description 14089 HEAD FEMORAL 28 SH LT 14090 HEAD FEMORAL 28 MD LT 14091 HEAD FEMORAL 28 LG LT 14094 HEAD FEMORAL 32 SH LT 14095 HEAD FEMORAL 32 MD LT 14096 HEAD FEMORAL 32 LG LT
- Z-0151-2026 — BioPro Femoral Head (Ceramic heads 28-30) Product ID/Description 19023 HEAD FEMORAL CERAMIC 28MM -3 19024 HEAD FEMORAL CERAMIC 28MM +0 19025 HEAD FEMORAL CERAMIC 32MM -3 19026 HEAD FEMORAL CERAMIC 32MM +0 19027 HEAD FEMORAL CERAMIC 32MM +3
- Z-0688-2022 — Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC M/L, Part ID 17037
- Z-0685-2022 — Titanium MPJ (Toe Implant)TOE JOINT TITANIUM NPC LG, Part ID 16816
- Z-0689-2022 — Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC LG, Part ID 17038
- Z-0686-2022 — Titanium MPJ (Toe Implant)TOE JOINT TITANIUM PC SM, Part ID 17035
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 Biopro, Inc.
- K163627 — Shotel Ankle Arthrodesis Nail System
- K162674 — BioPro Foot Plating Systems
- K132510 — BIOPRO - INFINITY PLATE ANCHOR SYSTEM
- K130298 — BIOPRO KWICK-WIRE UNIVERSAL SCREW SYSTEM
- K121973 — BIOPRO HEMI-EDGE TOE SYSTEM
- K100761 — BIOPRO POLAR HEAD
- K101030 — MODIFICATION TO HBS HEADLESS BONE SCREW
- K090208 — BIOPRO FEMORAL HEADS
- K083490 — BIOPRO K-WIRE, MODELS 16863, 17231, 17232, 18577, 18682-18685
- K082705 — BIOPRO BIPOLAR HEAD, MODELS 18130-18152
- K081149 — BIOPRO GO-EZ SCREW
- K072298 — BIOPRO MEMORY STAPLE, MODELS 18062-18073
- K061798 — BIOPRO MEMORY STAPLE
- K061089 — MODULAR THUMB IMPLANT, MODELS 17600, 17601, 17602, 17603, 17596, 17597, 17598, 17599
- K052596 — MODULAR THUMB IMPLANT, MODELS 17065,17066,17243,17067,17199,17238,17005,17239,17006,17240,17007,17241,17500,17501,17507
- K043542 — BIOPRO TARA FEMORAL RESURFACING COMPONENT
- K041595 — TOE MP JOINT, MODELS 10412-10414, 14958, 14960, 1060-10062,16818,-16822,16867-16870
- K041936 — BIOPRO SUBTALAR IMPLANT
- K011459 — WUJIN #3 FEMORAL BONE PLATE
- K011460 — WUJIN #3 TIBIAL BONE PLATE
- K010149 — WUJIN #3 FEMORAL NAIL
- K001046 — BIOPRO GLENOID COMPONENT W/ KEEL & W/ POSTS
- K990821 — PROVIDENCE CUP SYSTEM
- K960467 — POWDER FREE LATEX EXAMINATION GLOVE
- K922500 — PSL TOTAL HIP REPLACEMENT SYSTEM
- K925682 — BIOPRO ZIRALLOY MODULAR FEMORAL HEADS, MODIFIED
- K922841 — BIOPRO MODULAR TIBIAL TRAY
- K920145 — BIOPRO DRG CUSTOM HIP REPLACEMENT SYSTEM
- K912641 — BIOPRO ZIRALLOY MODULAR FEMORAL HEADS
- K911378 — TOWNLEY GREAT TOE JOINT
- K904448 — TOWNLEY TOTAL KNEE (TTK)
- K910352 — BIOPRO METAL BACKED CEMENTED ACETABULAR CUP
- K904207 — BIOPRO TRINITY ACETABULAR CUP
- K895886 — BIOPRO HEMI-ENDO MODULAR HEAD FOR PSL SYSTEM
- K894604 — BIOPRO PROXIMAL FEMORAL ARTICULAR REPLACEMENT
- K890044 — BIOPRO ANATOMIC UNICOMPARTMENTAL KNEE
- K882869 — TOWNLEY COX COMB ACETABULAR COMPONENT
- K882146 — BIOPRO PC FEMORAL HIP COMPONENT
- K874099 — REGENT DISPO STERILE BIOGEL STARCH FREE SURG GLOVE
- K872535 — BIOPRO FEMORAL HIP COMPONENT
- K872856 — BIOPRO 32MM BALL
Data sourced from openFDA. This site is unofficial and independent of the FDA.