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BioPro, Inc.

8 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
BioPro Femoral Head (Metal 22, 28, 32, 36, 40) cobalt chromium and ceramic heads Part ID/D recall (Z-0148-2026)BioPro, Inc.2025-10-14
BioPro Endo Head (Metal uni-polar, 38-55) Product Number/Description 10179 ENDO MD 38 1018 recall (Z-0149-2026)BioPro, Inc.2025-10-14
BioPro Bipolar Head Product ID/Description 18130 BIPOLAR HEAD 38MM 18131 BIPOLAR HEAD 39MM recall (Z-0150-2026)BioPro, Inc.2025-10-14
BioPro Femoral Head (Ceramic heads 28-30) Product ID/Description 19023 HEAD FEMORAL CERAMI recall (Z-0151-2026)BioPro, Inc.2025-10-14
BioPro Endo Head (Ceramic) Product ID/Description 13006 ENDO MODULAR CERAMIC SH 38 13012 E recall (Z-0152-2026)BioPro, Inc.2025-10-14
BioPro Femoral Head Product ID/Description 14089 HEAD FEMORAL 28 SH LT 14090 HEAD FEMORAL recall (Z-0153-2026)BioPro, Inc.2025-10-14
BioPro Femoral Head 28 mm -6 mm, Item 19003. Orthopedic femoral head for implantation. recall (Z-0163-2012)Biopro, Inc.2011-11-04
BioPro Femoral Head 28 mm +18, Item 19010. Orthopedic femoral head for implantation recall (Z-0164-2012)Biopro, Inc.2011-11-04

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Every clearance here is in the API, with alerts when new ones post.