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Sign in to claim this brandHENRY SCHEIN, INC.
United States·US-MF-000021683
Last updated May 30, 2026
Information
- Country
- United States
- Address
- 135, Duryea Road, Melville, United States
- Website
- henryschein-dental.de
- —
- —
- [email protected]
- Phone
- +1(732)918-0770
- PRRC Contact
- Tracey Alexander
- EUDAMED SRN
- US-MF-000021683
- FDA FEI Number
- —
- DUNS Number
- 012430880
Catalogue (11454)
Page 230 of 230| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Henry Schein | 9884183 | EUDAMED | Class I | Active |
| Henry Schein | 9003223 | EUDAMED | Class I | Active |
| Henry Schein | 9009542 | EUDAMED | Class I | Active |
| Henry Schein | 9001069 | EUDAMEDFDA UDI | Class I | Active |
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FDA Recalls (3)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Nov 10, 2011 | Z-0390-2012 | — | terminated | The specific lots of Maxcem Elite Refill Kit appear not to be authentic. |
| Jun 27, 2003 | Z-1046-03 | — | terminated | FDA's analysis revealed defects (holes) in the latex gloves. |
| Jun 27, 2003 | Z-1045-03 | — | terminated | FDA's analysis revealed defects (holes) in the latex gloves. |