Home › Device types › LYQ
Accessories, Fixation, Spinal Intervertebral Body
FDA product code LYQ · Class 1 · Orthopedic
229
Registered devices
9
Adverse events
2
Recalls
3
510(k) clearances
Devices with this code
RIVA Pedicle Screw System — XENIX MEDICAL LLCDistraction Screw, 14MM pouch — MEDLINE INDUSTRIES, INC.INTEGRATE-C — Happe Spine, LLCSureMAX-SA — ADDITIVE IMPLANTS, LLCPTS — Pt. Solutions, LLCSureMAX-SA — ADDITIVE IMPLANTS, LLCINTEGRATE-C — Happe Spine, LLCINTEGRATE-C — Happe Spine, LLCPTS — Pt. Solutions, LLCKeyLift™ — FLOSPINE LLCINTEGRATE-C — Happe Spine, LLCKeyLift™ — FLOSPINE LLCINTEGRATE-C — Happe Spine, LLCINTEGRATE-C — Happe Spine, LLCINTEGRATE-C — Happe Spine, LLCINTEGRATE-C — Happe Spine, LLCINTEGRATE-C — Happe Spine, LLCDistraction Screw — MEDLINE INDUSTRIES, INC.INTEGRATE-C — Happe Spine, LLCINTEGRATE-C — Happe Spine, LLCINTEGRATE-C — Happe Spine, LLCSureMAX — ADDITIVE IMPLANTS, LLCINTEGRATE-C — Happe Spine, LLCSureMAX — ADDITIVE IMPLANTS, LLC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-05-10 | Zimmer Biomet Spine Inc. | Zimmer Biomet is conducting a medical device recall for Vitality T27 Final Drivers and Vitality Torque Limiting Handle 90 in-lbs because when applying torque t |
| 2015-01-13 | Medtronic Sofamor Danek USA Inc | The product, labeled as containing, one bevel-tipped instrument and one diamond-tipped instrument, may contain either two bevel-tipped instruments or two diamon |
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