338 results · 30ms · Sources: EU EUDAMED, US FDA

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NON-PYROGENIC ULTRASOUND TRANSDUCER COVER

FDA 510(k)
FDA Class 2 ·Radiology

CoRoent

FDA UDI
Nuvasive, Inc.·00887517597281·CoRoent Large MP Ti, 15x9x28mm 12°

Millennium

FDA UDI
Avalign Technologies, Inc.·00190776399733·Flexible Rat Tooth Grasping Forceps, 3fr, 115cm WL

LINK Instruments - Trial implants and size gauges

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575411474·Orthopaedic prosthesis instrument, reusable - G...

LINK Instruments - Trial implants and size gauges

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575411498·Orthopaedic prosthesis instrument, reusable - G...

LINK Instruments - Trial implants and size gauges

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575414369·Femoral stem prosthesis trial - SPII Model Lubi...

LINK Instruments - Trial implants and size gauges

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575411481·Orthopaedic prosthesis instrument, reusable - G...

LINK Instruments - Trial implants and size gauges

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575411504·Orthopaedic prosthesis instrument, reusable - G...

LINK Instruments - Trial implants and size gauges

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575414383·Femoral stem prosthesis trial - SPII Model Lubi...

3M COMPLY LEAD FREE PROCESS INDICATORS FOR STEAM

FDA 510(k)
FDA Class 2 ·General Hospital

PIONEER ASPECT ANTERIOR CERVICAL PLATE MODEL 24-SERIES

FDA 510(k)
FDA Class 2 ·Orthopedic

KIT PREPMATE CONSUME 480 TEST

FDA Adverse Event
Malfunction ·Product code MKQ·October 13, 2021

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017