LinkBio Corp.
LinkBio Corp. holds FDA 510(k) medical device clearances, first cleared 2019, most recent 2025, with 50 FDA device recalls on record.
Top product codes for LinkBio Corp.
FDA recalls by LinkBio Corp.
10 most recent of 50- Z-1810-2026 — LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.
- Z-1674-2023 — LINK SymphoKnee System L-Shaped Femoral Augment, Medial-Right/Lateral-Left, Sz 5-6 Tilastan, cemented. Intended for primary and revision total knee replacement. Item Number: 880-325/13
- Z-1534-2023 — LINK SLED Knee System ENDO MODEL SLED TIBIAL COMP 11 MM X 55 MM Item Number: 15-2030/11
- Z-1508-2023 — LINK SLED Knee System: ENDO SLED KNEE FEM COMP, MEDIUM SMALL Item Number: 15-2020/46
- Z-1549-2023 — LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP 9 MM X 55 MM Item Number: 15-2230/10
- Z-1543-2023 — LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP 9 MM X 45 MM Item Number: 15-2230/02
- Z-1552-2023 — LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP 8 MM X 45 MM Item Number: 15-2230/13
- Z-1536-2023 — LINK SLED Knee System ENDO MODEL SLED TIBIAL COMP 8 MM X 45 MM Item Number: 15-2030/13
- Z-1538-2023 — LINK SLED Knee System ENDO MODEL SLED TIBIAL COMP 8 MM X 55 MM Item Number: 15-2030/15
- Z-1522-2023 — LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 13MM X 55MM Item Number: 15-2028/12
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 LinkBio Corp.
Data sourced from openFDA. This site is unofficial and independent of the FDA.