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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 5 of 230
DeviceModel / ReferenceRegistriesClassStatus
Henry Schein 5703045
FDA UDI
Class IIActive
Henry Schein 5700892
FDA UDI
Class IActive
Henry Schein 1015161
FDA UDI
Class IActive
Channels 2020543
FDA UDI
Class IActive
Henry Schein 9004714
FDA UDI
Class IActive
Henry Schein 5701752
FDA UDI
Class IActive
Henry Schein 5701037
FDA UDI
Class IActive
Henry Schein 5700773
FDA UDI
Class IActive
Channels 2020094
FDA UDI
Class IActive
Henry Schein 1126711
FDA UDI
Class IActive
Henry Schein 1047423
FDA UDI
Class IIActive
Henry Schein 1001109
FDA UDI
Class IActive
Zirlux 9011335
FDA UDI
Class IIActive
Henry Schein 1000172
FDA UDI
Class IActive
Henry Schein 9007067
FDA UDI
Class IActive
Henry Schein 5701256
FDA UDI
Class IActive
Henry Schein 1125736
FDA UDI
Class IActive
Henry Schein 5701258
FDA UDI
Class IActive
Henry Schein 5703525
FDA UDI
Class IIActive
Henry Schein 9008059
FDA UDI
Class IActive
Henry Schein 1125161
FDA UDI
Class IActive
Henry Schein 1125207
FDA UDI
Class IActive
Henry Schein 5703795
FDA UDI
Class IIActive
Henry Schein 9012005
FDA UDI
Class IIActive
Henry Schein 1025543
FDA UDI
Class IActive
Henry Schein 5703330
FDA UDI
Class IActive
Henry Schein 5703151
FDA UDI
Class IActive
Maxi-Gard 5702300
FDA UDI
Class IActive
Henry Schein 9007525
FDA UDI
Class IActive
Henry Schein 9004882
FDA UDI
Class IActive
Henry Schein 9011553
FDA UDI
Class IIActive
Henry Schein 1126088
FDA UDI
Class IIActive
Henry Schein 1065757
FDA UDI
Class IActive
Henry Schein 1005638
FDA UDI
Class IActive
Henry Schein 1003175
FDA UDI
Class IActive
Henry Schein 5705449
FDA UDI
Class IIActive
Henry Schein 5703153
FDA UDI
Class IActive
Henry Schein 5702778
FDA UDI
Class IActive
Henry Schein 5702638
FDA UDI
Class IActive
Henry Schein 8882388
FDA UDI
Class IIActive
Henry Schein 9012044
FDA UDI
Class IIActive
Henry Schein 5700964
FDA UDI
Class IActive
Henry Schein 1015630
FDA UDI
Class IActive
Henry Schein 5700758
FDA UDI
Class IActive
Zirlux 901-0412
FDA UDI
Class IIActive
Henry Schein 5703862
FDA UDI
Class IIActive
Henry Schein 5702807
FDA UDI
Class IActive
Henry Schein 1126026
FDA UDI
Class IActive
Henry Schein 8882579
FDA UDI
Class IIActive
Henry Schein 1046500
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.