93 results · 23ms · 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.

AcuPulse W CO2 Laser Systems, Delivery Devices and Accessories

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

Joystick LH - IIA

FDA UDI
Aktormed GmbH·04260463844283·

Blade Scalpel

FDA UDI
KATENA PRODUCTS, INC.·00841668113554·IMPLANT BLADE 5.2MM (BX/5)

Blade Scalpel

FDA UDI
KATENA PRODUCTS, INC.·00841668113547·SLIT BLADE 3.2MM ANGLED (BX/5)

QUANTITATIVE BLOOD POOL SPECT (QBS)

FDA 510(k)
FDA Class 2 ·Radiology

WUNDER TEST

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

INFUSION DEVICES - UNKNOWN - IDD

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·November 6, 2024

AUTOSOFT XC

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·July 11, 2024

AUTOSOFT 90

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·July 14, 2024

AUTOSOFT XC

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·July 11, 2024

AUTOSOFT 90

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·July 14, 2024

NEUROMARK SYSTEM

FDA Adverse Event
Injury ·NEURENT MEDICAL LTD.·Product code GEI·November 26, 2024

AUTOSOFT XC

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·July 23, 2024

AUTOSOFT 90

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·June 9, 2024

MIO ADVANCE

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·August 3, 2024

AUTOSOFT XC

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·July 23, 2024

MIO ADVANCE

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·August 3, 2024

MIO ADVANCE

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·August 3, 2024

MIO ADVANCE

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·August 3, 2024

AUTOSOFT XC

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·August 8, 2024