93 results · 18ms · Sources: EU EUDAMED, US FDA

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PREMISE, PART NO. 32678, 10 PACK UNIDOSE PREMISE TRANS CLEAR, dental composite

FDA Recall
Terminated ·Kerr Corp·Product code EBF·September 5, 2008

PREMISE KIT, PART NO. 33882, UNIDOSE PREMISE MINI KIT, dental composite

FDA Recall
Terminated ·Kerr Corp·Product code EBF·September 5, 2008

PREMISE, PART NO. 32673, 10 PACK UNIDOSE PREMISE B2 OPAQUE, dental composite

FDA Recall
Terminated ·Kerr Corp·Product code EBF·September 5, 2008

PREMISE, PART NO. 32665, 10 PACK UNIDOSE PREMISE D4, dental composite

FDA Recall
Terminated ·Kerr Corp·Product code EBF·September 5, 2008

Herculite Ultra (Part Number 34333), dental composite resorative material. Manufactured by Kerr Corporation, Orange, CA.

FDA Recall
Terminated ·Sybron Dental Specialties·Product code EBF·February 23, 2009

PREMISE, PART NO. 32818, 10 PACK UNIDOSE PREMISA B3 (INTERNATIONAL ONLY), dental composite

FDA Recall
Terminated ·Kerr Corp·Product code EBF·September 5, 2008

PREMISE, PART NO. 32655, 10 PACK UNIDOSE PREMISE B1, dental composite

FDA Recall
Terminated ·Kerr Corp·Product code EBF·September 5, 2008

PREMISE, PART NO. 32817, 10 PACK UNIDOSE PREMISA B2 (INTERNATIONAL ONLY), dental composite

FDA Recall
Terminated ·Kerr Corp·Product code EBF·September 5, 2008

PREMISE, PART NO. 32663, 10 PACK UNIDOSE PREMISE D2, dental composite

FDA Recall
Terminated ·Kerr Corp·Product code EBF·September 5, 2008

PREMISE, PART NO. 32668, 10 PACK UNIDOSE PREMISE A2 OPAQUE, dental composite

FDA Recall
Terminated ·Kerr Corp·Product code EBF·September 5, 2008

37% Etching Gel-1ml syringe, part # T06 The intended use of these devices is to etch tooth dentin/enamel in order to prepare the tooth surface prior to the application of a bonding agent.

FDA Recall
Terminated ·Kerr/pentron Dba Kerr Corporation And Pentron Clinical·Product code EBF·March 31, 2011

ADVIA Centaur Calibrator C-Used with the ADVIA Centaur Ferritin assay on the ADVIA Centaur CP system only. (In-Vitro Diagnostic) Catalog Number: 672182005 (US Reference 6 pack)

FDA Recall
Terminated ·Siemens Healthcare Diagnostics, Inc·Product code DBF·October 9, 2012

Dimension Vista Ferritin (FERR) Flex reagent cartridge

FDA Recall
Terminated ·Siemens Healthcare Diagnostics, Inc.·Product code DBF·March 21, 2017