349 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BAUSCH + LOMB PROCOMFORT (SAMFILCON A) CONTACT LENS, BAUSCH + LOMB PROCOMFORT (SAMFILCON A) CONTACT LENS FOR PRESBYOPIA,
FDA 510(k)
FDA Class 2
·Ophthalmic
Trivicta
FDA UDI
Ortho Development Corporation·00822409123865·Collar EXT Size 8
OneLIF™
FDA UDI
Novapproach Spine LLC·G07001111312080·Trial-OneLIF Interbody, Small, 13 Degree, 12mm ...
OneLIF™
FDA UDI
Novapproach Spine LLC·G07001191312080·Bullet Trial, 12 mm AH - 08 mm PH
OneLIF™
FDA UDI
Novapproach Spine LLC·G07001011312080·OneLIF Interbody, Small, 13 Degree, 12mm X 8mm
GAL-1A BLOOD GLUCOSE MONITORING SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Chemistry
REAADS IGM ANTI-B2GPI TEST KIT, MODEL 038-001
FDA 510(k)
FDA Class 2
·Immunology
VACUTRON
FDA UDI
Allied Medical, LLC·00026072005446·CONTINUOUS SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072005453·CONTINUOUS SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072005484·CONTINUOUS SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072005460·CONTINUOUS SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072005491·CONTINUOUS SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072005477·CONTINUOUS SUCTION REGULATORS
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