332 results · 35ms · 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.

OVATION 10/12 HIP STEM

FDA 510(k)
FDA Class 2 ·Orthopedic

Pro-Link Ti

FDA UDI
Life Spine, Inc.·00190837081010·

ELMED

FDA UDI
ELMED INCORPORATED·00842180174870·GERALD Forceps, 1 x 2 teeth. Overall length 9in...

PULMOTRACK 5050 WHOLTER, MODEL 5050

FDA 510(k)
FDA Class 2 ·Cardiovascular

PROTEC-TOP, STERIDENT, BENTO

FDA 510(k)
FDA Class 2 ·General Hospital

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

OT VERIO PRO PLUS METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 1, 2014

NOVASURE IMPEDANCE CONTROLLED EA SYSTEM

FDA Adverse Event
Injury ·HOLOGIC·Product code MNB·May 10, 2013

PRECISION XTRA

FDA Adverse Event
Malfunction ·Product code NBW·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