21 results · 21ms · 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.

IMPACT, UNIVERSAL SINGLE-LIMB, VENTILATOR CIRCUIT, MODEL 820-0099-00

FDA 510(k)
FDA Class 2 ·Anesthesiology

nSpire Health

FDA UDI
NSPIRE HEALTH, INC.·10852417003689·KoKo Pulmonary Function Filter Kit, White with ...

16PW - Class A Burn 21 - Poly White

FDA UDI
Certified Safety Manufacturing, Inc.·00766588620626·16PW - Class A Burn 21 - Poly White

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112557·BARRON VACUUM TREPHINE 9.0MM

SPECTRA WAVEWRITER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·February 15, 2024

Persona® Trabecular Metal®

FDA UDI
Zimmer, Inc.·00889024470071·

Persona® Trabecular Metal®

FDA UDI
Zimmer, Inc.·00889024470088·

PERSONA™ Trabecular Metal™

FDA UDI
Zimmer, Inc.·00889024230170·

PERSONA™ Trabecular Metal™

FDA UDI
Zimmer, Inc.·00889024230187·

PF2

FDA 510(k)
FDA Class 2 ·Orthopedic

SAMSUNG 10DR IMPLANT SYSTEM

FDA 510(k)
FDA Class 2 ·Dental

MECHANICAL (MANUAL) WHEELCHAIR

FDA Adverse Event
JAEYONG·Product code IOR·March 26, 2013

SECURE II MED/SURG BED

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code INK·March 10, 2011

CODMAN UNIT AIR DRIV COM

FDA Adverse Event
Malfunction ·CODMAN & SHURTLEFF, INC.·Product code HBF·March 28, 2008

Barron Radial Vacuum Trephine (1) Complete Trephine Set 9.0mm Dia. Ref. K20-2062 Lot 122336 Opthalmic

FDA Enforcement
Class II ·Terminated·Surgical Instrument Service And Savings, Inc.·July 10, 2013

ASAHI PROWATER

FDA Adverse Event
Injury ·ASAHI INTECC CO., LTD.·Product code DQX·June 9, 2019

ASAHI PROWATER

FDA Adverse Event
Injury ·ASAHI INTECC CO., LTD.·Product code DQX·June 9, 2019

PERSONA 2 PEG POROUS TIBIAL COMPONENT

FDA Adverse Event
Injury ·ZIMMER INC·Product code MBH·November 17, 2015

Barron Radial Vacuum Trephine (1) Complete Trephine Set 9.0mm Dia. Ref. K20-2062 Lot 122336 Opthalmic

FDA Recall
Terminated ·Surgical Instrument Service And Savings, Inc.·Product code HRH·May 3, 2013

Daig Livewire Steerable, Product Number 401932; REPROCESSED ELECTROPHYSIOLOGY CATHETER

FDA Enforcement
Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026