45 results · 21ms · 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.

C.T.M. MOBILITY SCOOTER, MODEL H2-686, HS-740, HS-580

FDA 510(k)
FDA Class 2 ·Physical Medicine

CUSTOM PROCEDURE KIT

FDA UDI
MEDIVATORS INC.·40677964003705·Endo Carry-on Procedure Kit includes Enzymatic ...

intellijoint HIP®

FDA UDI
Intellijoint Surgical Inc·00628184003565·Femoral Disc, Nails, G2

electric toothbrush

FDA UDI
Access Dental Lab, LLC·00850007728052·powered toothbrush-Power toothbrush-Blurple-retail

CURE ACP

FDA UDI
SpineArt SA·07640270065052·ANTERIOR CERVICAL PLATE, 3 LEVELS L56

CURE™ ACP

FDA UDI
MEDITECH SPINE, LLC·B167700003560·

SPACELABS HEALTHCARE

FDA UDI
SPACELABS HEALTHCARE (WASHINGTON), INC·10841522121913·EP JUNCTION LEADSET,PM-3,US

BIO-LIPID HUMAN SERUM HDL AND LDL CALIBRATORS

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

SMART SHIELD NON-STERILE POWDER-FREE PEPPERMINT SCENTED GREEN LATEX EXAMINATION GLOVES

FDA 510(k)
FDA Class 1 ·General Hospital

CURE 2.0™ ACP

FDA UDI
MEDITECH SPINE, LLC·B167S11000003560·

CURE 2.0 ACP

FDA UDI
SpineArt SA·07640375231352·CERVICAL 3 LEVEL TEMPLATE L56

CURE 2.0™ ACP

FDA UDI
MEDITECH SPINE, LLC·B167T1000003560·

CURE ACP

FDA UDI
SpineArt SA·07640270065366·ANTERIOR CERVICAL PLATE, 3 LEVELS L56

CURE 2.0 ACP

FDA UDI
SpineArt SA·07640375233264·ANTERIOR CERVICAL PLATE, 3 LEVELS L56

CURE™ ACP

FDA UDI
MEDITECH SPINE, LLC·B167S1700003560·

MONOCRYL POLIGLECAPRONE 25 SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAN·June 24, 2019

MONOCRYL POLIGLECAPRONE 25 SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAN·June 24, 2019

INF SET NERIA GUARD 60CM 9MM

FDA Adverse Event
Malfunction ·INTRAPUMP INFUSION SYSTEMS / UNOMEDICAL A/S·Product code FPA·March 18, 2025

INF SET NERIA GUARD 60CM 9MM

FDA Adverse Event
Malfunction ·INTRAPUMP INFUSION SYSTEMS / UNOMEDICAL A/S·Product code FPA·March 18, 2025

IN TOUCH ZU

FDA Adverse Event
Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·March 12, 2013