Home › Ss White Burs, Inc. › EXIMIA7
EXIMIA7
Ss White Burs, Inc. · Model 050/06-H · UDI-DI 06976245260339
7
510(k) clearances
0
Adverse events
5
Recalls
86
Facilities
Description
EXEMIA 7 PAPER POINTS 50/.06 - 100 PACK
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-08-04 | Ultradent Products, Inc. | The barcode label was placed underneath the sterile barrier and the product was re-wrapped. |
| 2017-08-04 | Ultradent Products, Inc. | The barcode label was placed underneath the sterile barrier and the product was re-wrapped. |
| 2017-08-04 | Ultradent Products, Inc. | The barcode label was placed underneath the sterile barrier and the product was re-wrapped. |
| 2017-08-04 | Ultradent Products, Inc. | The barcode label was placed underneath the sterile barrier and the product was re-wrapped. |
| 2017-08-04 | Ultradent Products, Inc. | The barcode label was placed underneath the sterile barrier and the product was re-wrapped. |
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.