Home › Paonan Biotech Co.,Ltd. › “Paonan” Orthopedic Manual Surgical Instrument (Non-Sterile)
“Paonan” Orthopedic Manual Surgical Instrument (Non-Sterile)
Paonan Biotech Co.,Ltd. · Model 406-1201 · UDI-DI 04719878787055
5
510(k) clearances
160
Adverse events
1
Recalls
159
Facilities
Description
Rod Bender
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-06-22 | Synthes USA HQ, Inc. | A complaint was received of the tips of the Matrix 5.5.mm Left and Right Coronal Bender breaking while bending a spinal rod component of the Matrix System. |
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.