25 results · 20ms · 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.

EXCEL A.V FISUTAL NEEDLE SET

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450465301·

CosmoLock Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07311K0130300·Wrench, Derotation, Double Ended

MAGNIVISION

FDA UDI
FGX INTERNATIONAL INC.·00193033588888·

MAGNIVISION

FDA UDI
FGX INTERNATIONAL INC.·00193033588918·

MAGNIVISION

FDA UDI
FGX INTERNATIONAL INC.·00193033588895·

MAGNIVISION

FDA UDI
FGX INTERNATIONAL INC.·00193033588901·

CosmoLock Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07311K0130070·Rocker, One Piece

MAGNIVISION

FDA UDI
FGX INTERNATIONAL INC.·00193033588925·

MAGNIVISION

FDA UDI
FGX INTERNATIONAL INC.·00193033588932·

Phonak

FDA UDI
Phonak AG·07613275081143·Phonak Bolero Q50-M312 (blue transparent)

JEWEL CAST III

FDA 510(k)
FDA Class 2 ·Dental

DAUM DOUBLE-SHOOT BISOPSY GUN

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

INSPIRA SMOOTH SILICONE GEL FILLED BREAST IMPLANT

FDA Adverse Event
Injury ·ALLERGAN (COSTA RICA)·Product code FTR·July 11, 2024

SCHILLER

FDA Adverse Event
Malfunction ·SCHILLER AG·Product code MHX·November 2, 2006

VERTEBRAL SPACER-TR 10MMX27MM 11MM HEIGHT

FDA Adverse Event
Malfunction ·SYNTHES ELMIRA·Product code MQP·February 20, 2013

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 1, 2013

ACCU-CHEK FLEXLINK PLUS

FDA Adverse Event
Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code LZG·March 4, 2011

PLATE,FIXATION,BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HRS·August 15, 2014

SPECTRUM Pump, Model No. 35700BAX. Intended to be used for the controlled administration of intravenous fluids.

FDA Enforcement
Class II ·Terminated·Baxter Healthcare Corp.·October 8, 2014