334 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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