82 results · 27ms · 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.

TITANIUM CEMENT RESTRICTOR (TCR)

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

Premier Composite Instruments

FDA UDI
PREMIER DENTAL PRODUCTS COMPANY·00348783009774·CPF DE_S4

GEN4 DIGITAL

FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828113656·GEN4 DIGITAL

LINK Endo-Model EVO Knee System

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575274598·Replacement set, CoCrMo, UHMWPE, rotating hinge...

CHROMOSTREAK

FDA 510(k)
FDA Class 1 ·Microbiology

MILLENNIA ACUPUNCTURE NEEDLE

FDA 510(k)
FDA Class 2 ·General Hospital

NA

FDA UDI
Zimmer, Inc.·00889024067134·

PROLIFT PELVIC FLOOR REPAIR

FDA Adverse Event
Injury ·ETHICON, INC.·Product code FTL·June 22, 2006

PROLIFT PELVIC FLOOR REPAIR

FDA Adverse Event
Injury ·ETHICON, INC.·Product code FTL·June 22, 2006

PROLIFT PELVIC FLOOR REPAIR

FDA Adverse Event
Injury ·ETHICON, INC.·Product code FTL·June 22, 2006

PROLIFT PELVIC FLOOR REPAIR

FDA Adverse Event
Injury ·ETHICON, INC.·Product code FTL·June 22, 2006

AUTOPULSE NIMH BATTERY

FDA Adverse Event
Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·February 11, 2013

AIR DERMATOME KIT

FDA Adverse Event
Injury ·ZIMMER SURGICAL·Product code GFD·February 23, 2011

CROSSSAIL CORONARY DILATION CATHETER

FDA Adverse Event
Malfunction ·ABBOTT VASCULAR - CARDIAC THERAPIES·Product code LOX·February 19, 2008

POSTERIOR PELVIC FLOOR REPAIR

FDA Adverse Event
Injury ·ETHICON INC.·Product code OTP·April 12, 2021

POSTERIOR PELVIC FLOOR REPAIR

FDA Adverse Event
Injury ·ETHICON INC.·Product code OTP·December 29, 2021

PROLIFT PELVIC FLOOR REPAIR UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code OTP·June 1, 2021

ANTERIOR PELVIC FLOOR REPAIR S

FDA Adverse Event
Injury ·ETHICON INC.·Product code OTP·November 18, 2021

ANTERIOR PELVIC FLOOR REPAIR S

FDA Adverse Event
Injury ·ETHICON INC.·Product code OTP·November 20, 2022

GYNECARE MESH UNKNOWN

FDA Adverse Event
Injury ·ETHICON INC.·Product code FTM·February 11, 2021