803 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.

IMPLANTABLE CLIP

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

DTS-3000

FDA UDI
DAESUNG MAREF CO.,LTD.·08809315676533·IOP Sensor 1ea

MATHIEU NEEDLE HOLDER

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896093522·MATHIEU NEEDLE HOLDER TUNGSTEN CARBIDE SERRATED...

OsteoMed

FDA UDI
OSTEOMED LLC·00845694001496·17mm Right L Plate, 1.0mm Thick

XLTEK EVOKED POTENTIAL HEADBOX, MODEL EP-4-RP (PROPOSED)

FDA 510(k)
FDA Class 2 ·Neurology

GUTHRIE PRIME POWDER-FREE CHLORINATED PATIENT EXAMINATION GLOVES

FDA 510(k)
FDA Class 1 ·General Hospital

Widex

FDA UDI
Widex A/S·05706069553475·Widex UNIQUE U-FA BTE (Metallic Blue ) Telecoil...

Widex

FDA UDI
Widex A/S·05706069498509·Widex D-FA P (Metallic Blue ) Telecoil, Volume ...

PAINSMART IOD

FDA Adverse Event
Malfunction ·MOOG DEVICE GROUP·Product code FRN·April 29, 2013

ABGII NO4 CEMENTLESS LEFT V40

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MAY·September 18, 2014

TRANSTAR STRETCHER

FDA Adverse Event
Malfunction ·HILL-ROM INC.·Product code FPO·May 16, 2011

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·November 8, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 28, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 11, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 4, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 11, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 21, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 25, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 24, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 15, 2021