14 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.

JO Naturalove Personal Lubricant, JO Naturalove Strawberry Fields Flavored Personal Lubricant

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

SSW CARBIDE GREAT WHITE

FDA UDI
Ss White Burs, Inc.·D6901821052·GREAT WHITE GOLD CARBIDE GW330 - 5 PACK

Ophthalmic Retractor

FDA UDI
KATENA PRODUCTS, INC.·00841668100967·DESMARRES LID RETRACTOR #1

SMI CARDIOVASCULAR PATCH

FDA 510(k)
FDA Class 2 ·Cardiovascular

PERCLOT TOPICAL

FDA 510(k)
FDA Unclassified ·Unknown

GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·July 6, 2017

GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·July 6, 2017

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

FDA Adverse Event
Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·October 17, 2014

AUTOLUBE-III

FDA Adverse Event
Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code GEY·June 21, 2013

DELTA XL

FDA Adverse Event
Malfunction ·DRAEGER MEDICAL SYSTEMS, INC. (IT/M)·Product code MHX·June 23, 2011

UNKNOWN

FDA Adverse Event
Malfunction ·WILLIAM COOK EUROPE·Product code DTK·October 23, 2017

UNKNOWN

FDA Adverse Event
Malfunction ·WILLIAM COOK EUROPE·Product code DTK·October 23, 2017

GUNTHER TULIP NAVALIGN FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·October 20, 2017

MultiDiagnost Eleva; x-ray system. Product Codes: 708032, 708036

FDA Enforcement
Class II ·Terminated·Philips Electronics North America Corporation·August 10, 2016