44 results · 22ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

DURACON SYMMETRIC METAL-BACKED PATELLAR COMPONENT

FDA 510(k)
FDA Class 2 ·Orthopedic

Henry Schein

FDA UDI
HENRY SCHEIN, INC.·00304040043646·Curette Gracey DE 13/14

Jade

FDA UDI
DHARMA RESEARCH, INC.·00353045002134·Jade Green 37% Phosphoric Acid Etchant Gel - 1 ...

THORATEC® VAD, LVAD PNEUMATIC EXTENSION LEAD, 7 FT

FDA UDI
Thoratec Corporation·00813024012627·

MODIFIED HYDROPHILIC COATED GUIDEWIRE

FDA 510(k)
FDA Class 2 ·Cardiovascular

WALLGRAFT TRACHEOBRONCHIAL ENDOPROSTHESIS AND UNISTEP DELIVERY SYSTEM

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

LUMIRADX SARS-COV-2 AG TEST STRIP KIT

FDA Adverse Event
Malfunction ·LUMIRADX UK LTD.·Product code QKP·May 13, 2021

LUMIRADX SARS-COV-2 AG TEST STRIP KIT

FDA Adverse Event
Malfunction ·LUMIRADX UK LTD.·Product code QKP·May 13, 2021

LUMIRADX SARS-COV-2 AG TEST STRIP KIT

FDA Adverse Event
Malfunction ·LUMIRADX UK LTD.·Product code QKP·May 13, 2021

3DKNEE

FDA Adverse Event
ENCORE MEDICAL, L.P.·Product code OIY·March 12, 2013

SECURE 2 MED/SURGBED

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FNL·February 18, 2011

S-ROM CUP ACE, ZTT-1 L32,56DP

FDA Adverse Event
Injury ·DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC·Product code LPH·February 18, 2008

BONE WAX 24X2.5G

FDA Adverse Event
Malfunction ·B.BRAUN SURGICAL SA·Product code MTJ·October 30, 2019

BONE WAX 24X2.5G

FDA Adverse Event
Malfunction ·B.BRAUN SURGICAL SA·Product code MTJ·May 7, 2019

LUMIRADX SARS-COV-2 AG TEST STRIP KIT

FDA Adverse Event
Malfunction ·LUMIRADX UK LTD·Product code QKP·November 7, 2022

LUMIRADX SARS-COV-2 AG TEST STRIP KIT

FDA Adverse Event
Malfunction ·LUMIRADX UK LTD·Product code QKP·November 7, 2022

LUMIRADX SARS-COV-2 AG TEST STRIP KIT

FDA Adverse Event
Malfunction ·LUMIRADX UK LTD·Product code QKP·November 7, 2022

LUMIRADX SARS-COV-2 AG TEST STRIP KIT

FDA Adverse Event
Malfunction ·LUMIRADX UK LTD·Product code QKP·November 7, 2022

LUMIRADX SARS-COV-2 AG TEST STRIP KIT

FDA Adverse Event
Malfunction ·LUMIRADX UK LTD·Product code QKP·December 1, 2022

LUMIRADX SARS-COV-2 AG TEST STRIP KIT

FDA Adverse Event
Malfunction ·LUMIRADX UK LTD·Product code QKP·November 7, 2022