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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 2 of 230
DeviceModel / ReferenceRegistriesClassStatus
Henry Schein 1011768
FDA UDI
Class IActive
Henry Schein 5700535
FDA UDI
Class IIActive
Henry Schein 9004315
FDA UDI
Class IActive
Zirlux 9011327
FDA UDI
Class IIActive
Henry Schein 1125147
FDA UDI
Class IActive
Henry Schein Maxima 1126585
FDA UDI
Class IActive
Henry Schein 1026657
FDA UDI
Class IActive
Henry Schein 1012096
FDA UDI
Class IActive
Henry Schein 1045496
FDA UDI
Class IActive
Henry Schein 5700567
FDA UDI
Class IActive
Henry Schein 5702930
FDA UDI
Class IIActive
Henry Schein 1001671
FDA UDI
Class IActive
Henry Schein 1061448
FDA UDI
Class IActive
Henry Schein 1011110
FDA UDI
Class IIActive
Henry Schein 5701665
FDA UDI
Class IIActive
Henry Schein 5700810
FDA UDI
Class IActive
Henry Schein 9011700
FDA UDI
Class IIActive
Henry Schein 1017092
FDA UDI
Class IIActive
Ionosphere 1009125
FDA UDI
Class IIActive
Henry Schein 1046328
FDA UDI
Class IActive
Henry Schein 9007151
FDA UDI
Class IActive
Henry Schein 9004734
FDA UDI
Class IActive
Henry Schein 1012919
FDA UDI
Class IActive
Henry Schein 1067577
FDA UDI
Class IActive
Henry Schein 5700711
FDA UDI
Class IActive
Henry Schein 1027437
FDA UDI
Class IActive
Henry Schein 5702831
FDA UDI
Class IIActive
Henry Schein 1007712
FDA UDI
Class IActive
Henry Schein 5702166
FDA UDI
Class IActive
Henry Schein 1013110
FDA UDI
Class IActive
Henry Schein 1009000
FDA UDI
Class IActive
Henry Schein 8882492
FDA UDI
Class IIActive
Henry Schein 1015802
FDA UDI
Class IActive
Henry Schein 9007993
FDA UDI
Class IIActive
Henry Schein 1063187
FDA UDI
Class IActive
Henry Schein Maxima 1125536
FDA UDI
Class IActive
Henry Schein 9004792
FDA UDI
Class IActive
Henry Schein 5702398
FDA UDI
Class IIActive
Henry Schein 5701528
FDA UDI
Class IIActive
Henry Schein 5701405
FDA UDI
Class IActive
Henry Schein 5703198
FDA UDI
Class IActive
Henry Schein 9792459
FDA UDI
Class IActive
Henry Schein 1006091
FDA UDI
Class IActive
Henry Schein 5700919
FDA UDI
Class IActive
Henry Schein 5700757
FDA UDI
Class IActive
Henry Schein 1011191
FDA UDI
Class IActive
Henry Schein 1005322
FDA UDI
Class IActive
Henry Schein 5703067
FDA UDI
Class IActive
Henry Schein 5703084
FDA UDI
Class IActive
Henry Schein 1067249
FDA UDI
Class IActive

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Importers

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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.