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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 9 of 230
DeviceModel / ReferenceRegistriesClassStatus
Henry Schein 9004717
FDA UDI
Class IActive
Henry Schein 9004578
FDA UDI
Class IActive
Henry Schein 9007372
FDA UDI
Class IActive
Henry Schein 5701497
FDA UDI
Class IIUnknown
Henry Schein 5702825
FDA UDI
Class IIActive
Henry Schein 5700768
FDA UDI
Class IActive
Henry Schein 1125075
FDA UDI
Class IActive
Henry Schein 5700924
FDA UDI
Class IActive
Henry Schein 1125679
FDA UDI
Class IActive
Henry Schein 9007608
FDA UDI
Class IActive
Henry Schein 9007649
FDA UDI
Class IIActive
Henry Schein 1047420
FDA UDI
Class IActive
Zirlux 9012412
FDA UDI
Class IIActive
Henry Schein 2020387
FDA UDI
Class IActive
Henry Schein 1125126
FDA UDI
Class IActive
Henry Schein 9011741
FDA UDI
Class IIActive
Henry Schein 5701958
FDA UDI
Class IIActive
Henry Schein 1124963
FDA UDI
Class IActive
Henry Schein 5702154
FDA UDI
Class IIActive
Henry Schein 1125996
FDA UDI
Class IActive
Henry Schein 1126001
FDA UDI
Class IIActive
Henry Schein 9007192
FDA UDI
Class IActive
Henry Schein 1126921
FDA UDI
Class IIActive
Henry Schein 2020348
FDA UDI
Class IActive
Henry Schein 9008058
FDA UDI
Class IActive
Henry Schein 2020080
FDA UDI
Class IActive
Channels 2020079
FDA UDI
Class IActive
Henry Schein 5703071
FDA UDI
Class IIActive
Henry Schein 1126808
FDA UDI
Class IActive
Henry Schein 1067408
FDA UDI
Class IActive
Criterion CR4G Chlor Glove 1127306
FDA UDI
Class IActive
Zirlux 9012391
FDA UDI
Class IIActive
Henry Schein 1048212
FDA UDI
Class IActive
Henry Schein 1065157
FDA UDI
Class IActive
Channels 2020098
FDA UDI
Class IActive
Henry Schein 5701286
FDA UDI
Class IActive
Henry Schein 9007115
FDA UDI
Class IActive
Troposphere 1001235
FDA UDI
Class IIActive
Henry Schein 1126906
FDA UDI
Class IActive
Henry Schein 5702008
FDA UDI
Class IIActive
Henry Schein 1002354
FDA UDI
Class IActive
Zirlux 9012631
FDA UDI
Class IIActive
Henry Schein 1063732
FDA UDI
Class IIActive
Henry Schein 1125278
FDA UDI
Class IActive
Henry Schein 1010285
FDA UDI
Class IActive
Henry Schein 5701066
FDA UDI
Class IIActive
Henry Schein 5703132
FDA UDI
Class IIActive
Zirlux 9010646
FDA UDI
Class IActive
Henry Schein 1009240
FDA UDI
Class IActive
Zirlux 901-0663
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.