Home › Corentec Co., Ltd › LOSPA IS Spinal System
LOSPA IS Spinal System
Corentec Co., Ltd · Model 20308202 · UDI-DI 08800017278148
HXQ
Prescription
0
510(k) clearances
13
Adverse events
1
Recalls
52
Facilities
Description
DLIF pin 10cm
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2014-09-26 | Biomet, Inc. | An investigation identified that high level friction may exist between the needle and Mamba suture passer instrument, causing the needle to break during use. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.