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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 4 of 230
DeviceModel / ReferenceRegistriesClassStatus
Henry Schein 8882482
FDA UDI
Class IIActive
Henry Schein 5702140
FDA UDI
Class IActive
Henry Schein 9011441
FDA UDI
Class IIActive
Henry Schein 1060434
FDA UDI
Class IActive
Henry Schein 5702812
FDA UDI
Class IActive
Henry Schein 1005170
FDA UDI
Class IActive
Henry Schein 5701788
FDA UDI
Class IActive
Henry Schein 1126142
FDA UDI
Class IActive
Henry Schein 5702875
FDA UDI
Class IActive
Henry Schein 5700737
FDA UDI
Class IIActive
Zirlux 9012600
FDA UDI
Class IIActive
Henry Schein 5705562
FDA UDI
Class IIActive
Henry Schein 1003046
FDA UDI
Class IActive
Nytrile XT PF Nitrile Glove 1104672
FDA UDI
Class IActive
Henry Schein 1005303
FDA UDI
Class IActive
Henry Schein 1000527
FDA UDI
Class IActive
Henry Schein 5702925
FDA UDI
Class IIActive
Henry Schein 1004121
FDA UDI
Class IActive
Henry Schein 1000018
FDA UDI
Class IActive
Henry Schein 1014846
FDA UDI
Class IActive
Zirlux 9012224
FDA UDI
Class IIActive
Henry Schein 9011207
FDA UDI
Class IIActive
Henry Schein 1008381
FDA UDI
Class IActive
Henry Schein 9011173
FDA UDI
Class IIActive
Natural Elegance 9004111
FDA UDI
Class IIActive
Henry Schein 9000998
FDA UDI
Class IIActive
Henry Schein 5705491
FDA UDI
Class IActive
Henry Schein 1127169
FDA UDI
Class IIActive
Henry Schein 1126081
FDA UDI
Class IIActive
Henry Schein 5702793
FDA UDI
Class IIActive
Henry Schein 9011036
FDA UDI
Class IIActive
Henry Schein 1002904
FDA UDI
Class IActive
Henry Schein 900-7476
FDA UDI
Class IIActive
Henry Schein 5703795
FDA UDI
Class IIActive
Henry Schein Acclean 5703744
FDA UDI
Class IActive
Henry Schein 9007773
FDA UDI
Class IActive
Henry Schein 1007488
FDA UDI
Class IActive
Henry Schein 5703209
FDA UDI
Class IActive
Henry Schein 9007923
FDA UDI
Class IActive
Henry Schein 1063928
FDA UDI
Class IActive
Henry Schein 9004780
FDA UDI
Class IActive
Henry Schein 5700940
FDA UDI
Class IActive
Henry Schein 5704392
FDA UDI
Class IIActive
Henry Schein 1003009
FDA UDI
Class IActive
Henry Schein 5700897
FDA UDI
Class IActive
Henry Schein 1019032
FDA UDI
Class IActive
Henry Schein 1008011
FDA UDI
Class IActive
Henry Schein 9007138
FDA UDI
Class IActive
Henry Schein 5703199
FDA UDI
Class IIActive
Henry Schein 9001889
FDA UDI
Class IActive

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.