Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Bodycad Laboratories, Inc.

FDA 510(k) & PMA Approved Devices — 16 products

Total Devices16
Categories3
Latest FDA decision2025-10-28
TypeNumberDevice NameCodeDateActions
510(k) K253300 Fine Osteotomy™HRS2025-10-28 View
510(k) K250394 Fine TTO™PBF2025-10-21 View
510(k) K250923 Fine Osteotomy™HRS2025-08-21 View
510(k) K241356 Fine Osteotomy™HRS2024-09-05 View
510(k) K240703 Fine Osteotomy™HRS2024-04-12 View
510(k) K240066 Fine Osteotomy™PBF2024-02-09 View
510(k) K231314 Fine Osteotomy™PBF2023-06-02 View
510(k) K212307 BC Reflex Uni Knee SystemHSX2021-10-12 View
510(k) K211895 BC Reflex Uni Knee SystemHSX2021-08-20 View
510(k) K211646 FINE OsteotomyHRS2021-07-28 View
510(k) K203697 BC Reflex Uni Knee SystemHSX2021-03-12 View
510(k) K193614 FINE Osteotomy around the kneeHRS2020-03-25 View
510(k) K191996 BC Reflex Uni Knee SystemHSX2019-12-05 View
510(k) K191150 Bodycad Unicompartmental Knee SystemHSX2019-10-08 View
510(k) K181302 Bodycad Unicompartmental Knee SystemHSX2019-01-17 View
510(k) K163700 Bodycad Unicompartmental Knee SystemHSX2017-03-29 View