Home › HENRY SCHEIN, INC. › Henry Schein
Henry Schein
HENRY SCHEIN, INC. · Model 1125900 · UDI-DI 00304040018286
NJM
Prescription
10
510(k) clearances
23
Adverse events
1
Recalls
47
Facilities
Description
Ceraket .018 Kit U/L 5x5 Roth HKS
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-11-19 | Ultradent Products, Inc. | Ultradent Products Inc. is recalling various lots of Avex CX2 Orthodontic Brackets because the design control process was not complete prior to distribution. |
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.