Home › DIO Corporation › UF(II) External Counter Sinker
UF(II) External Counter Sinker
DIO Corporation · Model NCS 5113 · UDI-DI 08800049201213
10
510(k) clearances
599
Adverse events
3
Recalls
190
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-04-14 | Straumann USA LLC | The referred batch was produced without the laser engraving of 7 mm. |
| 2017-07-10 | Zimmer Dental Inc | Zimmer Biomet is conducting a medical device field correction for various dental products due to several parts being shipped to the customer with only standard IFUs. All the produc |
| 2009-06-29 | Biomet 3i, LLC | Some of the packages of ACT3020, drills may actually contain an ACT3220 drill. |
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.