T.A.G. Medical Products Corporation, Ltd.
T.A.G. Medical Products Corporation, Ltd. holds FDA 510(k) medical device clearances, first cleared 2011, most recent 2026, with 7 FDA device recalls on record.
Top product codes for T.A.G. Medical Products Corporation, Ltd.
FDA recalls by T.A.G. Medical Products Corporation, Ltd.
- Z-2064-2023 — Betta Link LG Reusable ProngED Guide - Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number: 110045156
- Z-2065-2023 — Betta Link LG Reusable Fishmouth Guide-Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number: 110045157
- Z-2062-2023 — BETTA LINK SR REUSABLE PRONGED GUIDE- Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number: 110045150
- Z-2061-2023 — BETTA LINK LG KNOTLESS IMPLANT KIT-Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number: 110045160
- Z-2060-2023 — BETTA LINK SR KNOTLESS IMPLANT KIT-Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number:110045154
- Z-2063-2023 — BETTA LINK SR REUSABLE FISHMOUTH GUIDE-Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number: 110045151
- Z-1542-2020 — FlipCutter III Drill
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 T.A.G. Medical Products Corporation, Ltd.
- K253858 — GFS - Sterile Screws and Top Hat
- K231400 — Bladeless Trocar Artemis Lap Cannula
- K230058 — Bladeless Trocar Artemis Lap Cannula
- K221731 — FiberStitch Implant, Curved with two Polyester Implants and 2-0 FiberWire, FiberStitch Implant, Straight with two Polyester Implants and 2-0 FiberWire
- K210498 — Betta Link Knotless Implant System
- K202178 — VersaLoop Anchor System
- K190125 — FiberStitch Implant, Curved with two Polyester Implants and 2-0 FiberWire, FiberStitch Implant, Straight with two Polyester Implants and 2-0 FiberWire
- K143326 — T.A.G. Dental Implant System
- K142653 — G-Lok and G-Lok XL Extender
- K113297 — KNOTILUS ANCHOR SYSTEM
- K112296 — LATERAL BUTTON
- K110763 — LATARJET CORTICAL SCREW SET
Data sourced from openFDA. This site is unofficial and independent of the FDA.