42 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VERSACLOSE, MODEL VC-200-01
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DEBAKEY VASCULAR CLAMP
FDA UDI
SONTEC INSTRUMENTS, INC.·B09921005720·DEBAKEY PEDIATRIC VASCULAR CLAMP SPOON JAW
HS Stand. Burr, Ø7.0x70, 80k
FDA UDI
Bien-Air Surgery SA·17630055507133·
IN-OVATION® C
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K100552821·IN-OVATION® C EURO 022 U 5-5/L 3-3 CS-BC HK
IN-OVATION® C
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K100552811·IN-OVATION® C EURO 022 U5-5/L3-3 CS HK
IN-OVATION® C
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K100532601·IN-OVATION® C Roncone 022/U5-5 L3-3 CS HK
IN-OVATION® C
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K100532001·IN-OVATION® C Base Rx 022 U5-5/L3-3
IN-OVATION® C
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K100532611·IN-OVATION® C Roncone 022/U5-5 L3-3 CS-BC HK
IN-OVATION® C
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K100532111·IN-OVATION® C Base Rx 022 U5-5/L3-3 CS-BC HK
IN-OVATION® C
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K100532101·IN-OVATION® C Base Rx 022 U5-5/L3-3 CS HK
BD VISIDRAPE OPHTHALMIC DRAPES; BD VISIFLEX INCISE DRAPE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
E.N.S.I. SYRINGE
FDA 510(k)
FDA Class 2
·General Hospital
Widex
FDA UDI
Widex A/S·05706069437164·Widex SUPER440 S4-VS BTE (Winter silver/Black )...
Widex
FDA UDI
Widex A/S·05706069409857·Widex SUPER220 S2-VS BTE (Winter silver/Black )...
STEM: SMS SOLID SMS SOLID STEM STD SIZE 5
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·August 22, 2022
BD Q-SYTE CLOSED LUER ACCESS DEVICE
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FPA·April 29, 2025
BD Q-SYTE CLOSED LUER ACCESS DEVICE
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FPA·April 29, 2025
QUANTUM Q6 EDGE WITH TB3 POWER SEATING SYSTEM
FDA Adverse Event
Malfunction
·PRIDE MOBILITY PRODUCTS CORP·Product code IOR·September 24, 2015
ENDEAVOR RESOLUTE RX
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code NIQ·September 19, 2014
FEMORAL AND PROVISIONAL IMPACTOR/EXTRACTOR
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code MBH·May 17, 2011