30 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.

IHEALTH CLOUD

FDA 510(k)
FDA Class 2 ·Cardiovascular

COE-FLEX®

FDA UDI
Gc America Inc.·D6581312031·COE-FLEX® s Injection Type (base only)(1 x 90mL...

COE-FLEX®

FDA UDI
Gc America Inc.·10386040004893·COE-FLEX® s Injection Type (base only)(1 x 90mL...

N/A

FDA UDI
TETRA MEDICAL SUPPLY CORP.·00614138209275·NEOPRENE PATELLAR KNEE SUPPORT, LARGE

Trivicta

FDA UDI
Ortho Development Corporation·00822409123810·Collar EXT Size 3

e-scope® F.O. otoscope / ophthalmoscope LED 3.7 V,

FDA UDI
Rudolf Riester GmbH·04045396177062·The Riester otoscope is produced for illuminati...

Life Instruments

FDA UDI
Life Instrument Corporation·M93071312031C0·Custom Micro Curette 11.8" #3/0 Angled

Life Instruments

FDA UDI
Life Instrument Corporation·M93071312032C0·Custom Micro Curette 11.8" #3/0 rev ang.

Life Instruments

FDA UDI
Life Instrument Corporation·M93071312030C0·Custom Micro Curette 11.8" #3/0 straight

BIAX A.F. WRIST/BIAX ADVANCED FIXATION WRIST

FDA 510(k)
FDA Class 2 ·Orthopedic

TINA-QUANT ALBUMIN GEN 2

FDA 510(k)
FDA Class 2 ·Immunology

PROPHECY INFINITY

FDA Adverse Event
Malfunction ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code HSN·March 29, 2021

COOK® CERVICAL RIPENING BALLOON

FDA Adverse Event
Malfunction ·COOK INC·Product code PFJ·July 18, 2016

COOK® CERVICAL RIPENING BALLOON

FDA Adverse Event
Malfunction ·COOK INC·Product code PFJ·July 19, 2016

SHUNT SENSOR SYS500

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·May 23, 2013

SAPHIR 3

FDA Adverse Event
Injury ·MEDTRONIC S.A.·Product code NVZ·June 16, 2011

SUPERDIMENSION BRONCHUS SYSTEM (SDBS)

FDA Adverse Event
Death ·SUPERDIMENSION, LTD.·Product code JAK·August 20, 2008

ADVANCE 35 LP LOW PROFILE BALLOON CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code DQY·February 3, 2017

ADVANCE 35 LP LOW PROFILE BALLOON CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code DQY·March 10, 2017

PROPHECY INFINITY EU PATIENT SPECIFIC GUIDES

FDA Adverse Event
Injury ·WRIGHT MEDICAL TECHNOLOGY INC·Product code HSN·October 8, 2024