333 results · 21ms · Sources: EU EUDAMED, US FDA

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TI-1000 TRANSPORT INCUBATOR

FDA 510(k)
FDA Class 2 ·General Hospital

NA

FDA UDI
Stryker Leibinger GmbH & Co. KG·07613252599678·CUSTOMIZED MAND. RECON PLATE28, FULL

ihcDirect® PTH Ab, 5mL

FDA UDI
NOVODIAX, INC.·00850000596764·Clone C123

ihcDirect® PTH Ab, 15mL

FDA UDI
NOVODIAX, INC.·00850000596771·Clone C123

ihcDirect® PTH Ab Conjugate 15mL

FDA UDI
NOVODIAX, INC.·00850030934581·Clone C123

ihcDirect® PTH Ab Conjugate 5mL

FDA UDI
NOVODIAX, INC.·00850030934574·Clone C123

THE BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY

FDA 510(k)
FDA Class 2 ·Dental

PENTAX VIDEO BRONCHOSCOPES (EB FAMILY)

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·December 27, 2021

G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code MDS·May 23, 2014

SUREFIRE SCORPION NEEDLE

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code MDM·November 14, 2012

ATLAS PLUS DR

FDA Adverse Event
Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·September 10, 2010