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

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CorPath GRX System

FDA 510(k)
FDA Class 2 ·Cardiovascular

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112601·BARRON CORNEAL PUNCH 7.25MM

Blade Scalpel

FDA UDI
KATENA PRODUCTS, INC.·00841668113523·SLIT BLADE 3.0MM STR (BX/5)

Trifocus

FDA UDI
Diversified Products, Inc.·00037741220275·

Vilex Power Accessory

FDA UDI
VILEX IN TENNESSEE, INC.·00841731122308·KWire .078 x 9"(2.0x225mm))

DELTA 32; DELTA 32 TACT

FDA 510(k)
FDA Class 2 ·Radiology

THERMEDX 37-5 ELECTROCAUTERY PROBES, MODELS MPJ200, MPJ210, MPS220, MPN230, BPH240

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

DERMABOND PRINEO

FDA Adverse Event
Injury ·ETHICON - 3M / ETHICON, INC.·Product code OMD·October 21, 2022

TENDRIL SDX

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, INC., CARDIAC RHYTHM MANAGEMENT DIVISI·Product code NVN·January 13, 2014

PATROL PUMP

FDA Adverse Event
Malfunction ·ABBOTT NUTRITION·Product code LZH·August 5, 2011

MP70 INTELLIVUE PATIENT MONITOR

FDA Adverse Event
Death ·PHILIPS MEDICAL SYSTEMS·Product code DSI·June 24, 2013

UNKNOWN AVENIR STEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·June 8, 2022

UNKNOWN AVENIR STEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWY·June 8, 2022

UNKNOWN AVENIR STEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·June 8, 2022

UNKNOWN AVENIR STEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·June 8, 2022

UNKNOWN AVENIR STEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWY·June 8, 2022

UNKNOWN AVENIR STEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·June 8, 2022

UNKNOWN AVENIR STEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWY·June 8, 2022

UNKNOWN AVENIR STEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·June 8, 2022

UNKNOWN BROACH

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWY·June 8, 2022