341 results · 24ms · Sources: EU EUDAMED, US FDA

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RADVISION

FDA 510(k)
FDA Class 2 ·Radiology

CoRoent

FDA UDI
Nuvasive, Inc.·00887517597267·CoRoent Large MP Ti, 14x9x28mm 12°

Gyrus ACMI

FDA UDI
Gyrus ACMI, LLC·00821925030909·LARGE GENERIC INSTRUMENT MODULE 8.81” x 18.84”

OTSC (OVER-THE SCOPE-CLIP) SYSTEM SET

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

SYNTHES (USA) LARGE EXTERNAL FIXATION CLAMPS-MR SAFE

FDA 510(k)
FDA Class 2 ·Orthopedic

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

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·December 27, 2021

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

FDA Adverse Event
Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·October 1, 2014

BARD FLAT MESH

FDA Adverse Event
Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·May 9, 2013

THERA-I DR

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL, INC.·Product code DXY·June 16, 2011

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·October 15, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·June 17, 2022

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·December 27, 2021