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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 10 of 230| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Zirlux | 901-0582 | FDA UDI | Class II | Active |
| Henry Schein | 5701416 | FDA UDI | Class II | Active |
| Henry Schein | 5701557 | FDA UDI | Class I | Active |
| Henry Schein | 1126732 | FDA UDI | Class II | Active |
| Henry Schein | 5703619 | FDA UDI | Class I | Active |
| Criterion Nitrile EC | 1126788 | FDA UDI | Class I | Active |
| Henry Schein | 1125134 | FDA UDI | Class I | Active |
| Henry Schein | 5700921 | FDA UDI | Class I | Active |
| Henry Schein | 5701975 | FDA UDI | Class I | Active |
| Henry Schein | 1045767 | FDA UDI | Class I | Active |
| Henry Schein | 1066816 | FDA UDI | Class I | Active |
| Criterion N250 Nitrile PF Glove | 5700100 | FDA UDI | Class I | Active |
| Henry Schein | 1069882 | FDA UDI | Class I | Active |
| Henry Schein | 1027724 | FDA UDI | Class II | Active |
| Henry Schein | 1124861 | FDA UDI | Class II | Active |
| Henry Schein | 2020333 | FDA UDI | Class I | Active |
| Henry Schein | 1012452 | FDA UDI | Class I | Active |
| Nytrile XT PF Nitrile Glove | 1104671 | FDA UDI | Class I | Active |
| Henry Schein | 1000364 | FDA UDI | Class I | Active |
| Henry Schein | 5700165 | FDA UDI | Class I | Active |
| Henry Schein | 9011019 | FDA UDI | Class II | Active |
| Henry Schein | 1127363 | FDA UDI | Class I | Active |
| Henry Schein | 5702697 | FDA UDI | Class II | Active |
| Henry Schein | 9012059 | FDA UDI | Class II | Active |
| Henry Schein | 1045498 | FDA UDI | Class I | Active |
| Henry Schein | 1008350 | FDA UDI | Class II | Active |
| Henry Schein | 9011457 | FDA UDI | Class II | Active |
| Henry Schein | 9004765 | FDA UDI | Class I | Active |
| Henry Schein | 1004460 | FDA UDI | Class I | Active |
| Henry Schein | 1000261 | FDA UDI | Class I | Active |
| Henry Schein | 9004267 | FDA UDI | Class I | Active |
| Henry Schein | 5701008 | FDA UDI | Class I | Active |
| Henry Schein | 5700462 | FDA UDI | Class II | Active |
| Henry Schein | 1068958 | FDA UDI | Class II | Active |
| Henry Schein | 9004760 | FDA UDI | Class I | Active |
| Henry Schein | 9007316 | FDA UDI | Class I | Active |
| Henry Schein | 5702694 | FDA UDI | Class II | Active |
| Criterion N200 PF Nitrile | 9007440 | FDA UDI | Class I | Active |
| Henry Schein | 1047594 | FDA UDI | Class I | Active |
| Henry Schein | 5701950 | FDA UDI | Class I | Active |
| Henry Schein | 1004986 | FDA UDI | Class I | Active |
| Henry Schein | 9007050 | FDA UDI | Class I | Active |
| Henry Schein | 1026512 | FDA UDI | Class I | Active |
| Henry Schein | 1007457 | FDA UDI | Class I | Active |
| Henry Schein | 5700428 | FDA UDI | Class I | Active |
| Henry Schein | 5703047 | FDA UDI | Class II | Active |
| Henry Schein | 9004174 | FDA UDI | Class I | Active |
| Henry Schein | 1005706 | FDA UDI | Class I | Active |
| Henry Schein | 9011505 | FDA UDI | Class II | Active |
| Zirlux | 9012214 | FDA UDI | Class II | Active |
Related Companies
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Authorities
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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. |