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

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VALLEYLAB RETRACTABLE ELECTRODES

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

GEN4 INTERACTIVE

FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828189330·GEN4 INTERACTIVE

LP Low Profile

FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746086687·DB BKT LP UL BIC 022 T=0 A+3 R=0

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

3.5MM STARDRIVE CORTEX SCREW SELF-TAPPING 32MM

FDA Adverse Event
Injury ·SYNTHES MONUMENT·Product code HWC·January 28, 2013

UNKNOWN DEPUY ASR HIP

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·December 14, 2010