339 results
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35ms
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Sources: EU EUDAMED, US FDA
COLONGLIDE LUBRICANT
FDA 510(k)
FDA Class 1
·General Hospital
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587T1410280·14mm TLIF Implant 10mm Wide 28mm Length
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16721410280·
ELMED
FDA UDI
ELMED INCORPORATED·00842180170308·Single Ended Hegar Dilator, 28mm Tip, Autoclava...
Batrik Pin Kaps
FDA UDI
Batrik Medical Manufacturing Inc·00690521011120·Pin Guards, 0.028" (0.71 mm), Yellow, Non-sterile
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587T14102870·14mm TLIF Implant 10mm Wide 28mm Length 7 degrees
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1672141028060·
Batrik Pin Guard\.028"\Yellow w/sleeve
FDA UDI
Batrik Medical Manufacturing Inc·00690521014510·Pin Guards, 0.028" (0.71 mm), Yellow, Non-steri...
EUS BALLOON
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
CROWN DELTA HYDROPHILIC IMPRESSION MATERIAL
FDA 510(k)
FDA Class 2
·Dental
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
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·June 3, 2013