Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

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 13 of 230
DeviceModel / ReferenceRegistriesClassStatus
Henry Schein 2020085
FDA UDI
Class IActive
Henry Schein 1004058
FDA UDI
Class IActive
Henry Schein 1004137
FDA UDI
Class IActive
Henry Schein 1008026
FDA UDI
Class IActive
Henry Schein Tray Barriers 1014275
FDA UDI
Class IIActive
Henry Schein 5702177
FDA UDI
Class IIActive
Henry Schein 2021140
FDA UDI
Class IActive
Henry Schein 5705551
FDA UDI
Class IIActive
Henry Schein 1015188
FDA UDI
Class IIActive
Henry Schein 9011054
FDA UDI
Class IIActive
Henry Schein 1046399
FDA UDI
Class IActive
Zirlux 901-0786
FDA UDI
Class IIActive
Henry Schein 5702902
FDA UDI
Class IActive
Henry Schein 5702740
FDA UDI
Class IIActive
Henry Schein 1049639
FDA UDI
Class IActive
Henry Schein 5702615
FDA UDI
Class IIActive
Henry Schein 1125974
FDA UDI
Class IIActive
Henry Schein 1026077
FDA UDI
Class IActive
Henry Schein 1008187
FDA UDI
Class IIActive
Henry Schein 5700716
FDA UDI
Class IIActive
Henry Schein 9007246
FDA UDI
Class IActive
Henry Schein 1125073
FDA UDI
Class IActive
Henry Schein 9004726
FDA UDI
Class IActive
Henry Schein 1011858
FDA UDI
Class IActive
Henry Schein 5702120
FDA UDI
Class IIActive
Henry Schein 5701633
FDA UDI
Class IIActive
Henry Schein 9011111
FDA UDI
Class IIActive
Henry Schein 2020217
FDA UDI
Class IActive
Henry Schein 5750537
FDA UDI
Class IActive
Henry Schein 1125810
FDA UDI
Class IActive
Henry Schein 5702612
FDA UDI
Class IActive
Henry Schein 5705555
FDA UDI
Class IActive
Henry Schein 5703415
FDA UDI
Class IActive
Henry Schein 1060508
FDA UDI
Class IActive
Henry Schein 1003114
FDA UDI
Class IActive
Henry Schein 1067941
FDA UDI
Class IActive
Henry Schein 5702682
FDA UDI
Class IIActive
Henry Schein 1125526
FDA UDI
Class IActive
Henry Schein 5700283
FDA UDI
Class IActive
Henry Schein 1125150
FDA UDI
Class IActive
Henry Schein 5701495
FDA UDI
Class IIActive
Henry Schein 5702179
FDA UDI
Class IIActive
Henry Schein 9004318
FDA UDI
Class IActive
Henry Schein 5702158
FDA UDI
Class IIActive
Henry Schein 5703022
FDA UDI
Class IIActive
Henry Schein 1005244
FDA UDI
Class IActive
Henry Schein 5700186
FDA UDI
Class IActive
Nytrile X300 Electra Blue PF Nitrile 1127019
FDA UDI
Class IActive
Henry Schein Maxima 1126596
FDA UDI
Class IActive
Henry Schein 1125146
FDA UDI
Class IActive

Related Companies

Authorised Representatives

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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.