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HENRY SCHEIN, INC.

United States·US-MF-000021683

Last updated May 30, 2026

Information

Country
United States
Address
135, Duryea Road, Melville, United States
LinkedIn
—
Facebook
—
Phone
+1(732)918-0770
PRRC Contact
Tracey Alexander
EUDAMED SRN
US-MF-000021683
FDA FEI Number
—
DUNS Number
012430880

Catalogue (11454)

Page 6 of 230
DeviceModel / ReferenceRegistriesClassStatus
Henry Schein 5701816
FDA UDI
Class IActive
Henry Schein 1061228
FDA UDI
Class IActive
Henry Schein 9004673
FDA UDI
Class IActive
Henry Schein 1062223
FDA UDI
Class IActive
Zodiac 1032167
FDA UDI
Class IActive
Henry Schein 5700901
FDA UDI
Class IActive
Henry Schein 1004903
FDA UDI
Class IActive
Henry Schein 5700164
FDA UDI
Class IActive
Henry Schein 9007323
FDA UDI
Class IActive
Henry Schein 5703234
FDA UDI
Class IActive
Henry Schein 8882617
FDA UDI
Class IActive
Henry Schein 8882374
FDA UDI
Class IIActive
Henry Schein 1124853
FDA UDI
Class IIActive
Henry Schein 9011654
FDA UDI
Class IIActive
Henry Schein 5700933
FDA UDI
Class IActive
Zirlux 901-0659
FDA UDI
Class IIActive
Henry Schein 9007521
FDA UDI
Class IActive
Henry Schein 1002372
FDA UDI
Class IActive
Henry Schein 1126788
FDA UDI
Class IActive
Henry Schein 1007747
FDA UDI
Class IActive
Henry Schein 1047306
FDA UDI
Class IActive
ZCAD TempEsthetic 9007855
FDA UDI
Class IActive
Channels 2020616
FDA UDI
Class IActive
Henry Schein 5700708
FDA UDI
Class IActive
Henry Schein 9007991
FDA UDI
Class IIActive
Henry Schein 5703131
FDA UDI
Class IIActive
Zirlux 9010447
FDA UDI
Class IIActive
Henry Schein 1125145
FDA UDI
Class IActive
Henry Schein 1048600
FDA UDI
Class IIActive
Henry Schein 5701888
FDA UDI
N/AActive
Henry Schein 5701034
FDA UDI
Class IActive
Henry Schein 5702782
FDA UDI
Class IActive
Henry Schein 9004455
FDA UDI
UActive
Henry Schein 2020201
FDA UDI
Class IActive
Zirlux 9010832
FDA UDI
Class IActive
Henry Schein 5703927
FDA UDI
Class IIActive
Henry Schein 5703435
FDA UDI
Class IActive
Maxi-Gard 5702341
FDA UDI
Class IActive
Henry Schein 9004947
FDA UDI
Class IActive
Henry Schein 5703578
FDA UDI
Class IActive
Henry Schein 5703507
FDA UDI
Class IIActive
Maxi-Gard 5702337
FDA UDI
Class IActive
Henry Schein 5703313
FDA UDI
Class IActive
Henry Schein 5704226
FDA UDI
Class IIActive
Zirlux 901-0423
FDA UDI
Class IIActive
Henry Schein 9004930
FDA UDI
Class IActive
Maxima 1127260
FDA UDI
Class IIActive
Henry Schein 1045522
FDA UDI
Class IActive
Henry Schein 9011068
FDA UDI
Class IIActive
Henry Schein 1012587
FDA UDI
Class IIActive

Related Companies

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Importers

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Notified Bodies

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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.

DateRecall No.ClassStatusReason
Nov 10, 2011Z-0390-2012—terminated

The specific lots of Maxcem Elite Refill Kit appear not to be authentic.

Jun 27, 2003Z-1046-03—terminated

FDA's analysis revealed defects (holes) in the latex gloves.

Jun 27, 2003Z-1045-03—terminated

FDA's analysis revealed defects (holes) in the latex gloves.