190 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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WAGNER CONE PROSTHESIS
FDA 510(k)
FDA Class 2
·Orthopedic
SOLIDEA
FDA UDI
CALZIFICIO PINELLI SRL·08300496032380·PERSONALITY 70 SHEER, SIZE 2XXL, VISONE, GRADUA...
Baltic Denture System BD Load
FDA UDI
Merz Dental GmbH·D7091032380·Baltic Denture System BDLoad Mw7 PLSEbim6DFm A4...
nSpire Health
FDA UDI
NSPIRE HEALTH, INC.·00852417003118·Bronchial Challenge Kit, Disposable (single pat...
BUSCH®, BNA®
FDA UDI
BUSCH & CO. GmbH & Co. KG·D8120323801·Diamond, cylinder round, COOL DIAMANT, coarse g...
Ophthalmic Spatula
FDA UDI
KATENA PRODUCTS, INC.·00841668102749·BRIERLEY NUCLEUS SPLITTER
OPUS SMARTSTITCH SUTURE DEVICE
FDA Adverse Event
Other
·ARTHROCARE CORPORATION·Product code KOG·August 3, 2011
OPUS SMARTSTITCH M-CONNECTOR
FDA Adverse Event
Other
·ARTHROCARE CORPORATION·Product code KOG·August 3, 2011
OPUS SMARTSTITCH M-CONNECTOR
FDA Adverse Event
Other
·ARTHROCARE CORP.·Product code KOG·August 3, 2011
OPUS SMARTSTITCH SUTURE CARTRIDGE
FDA Adverse Event
Other
·ARTHROCARE CORPORATION·Product code KOG·August 3, 2011
OPUS SMARTSTITCH SUTURE CARTRIDGE
FDA Adverse Event
Other
·ARTHROCARE CORPORATION·Product code KOG·August 3, 2011
OPUS SMARTSTITCH M-CONNECTOR
FDA Adverse Event
Other
·ARTHROCARE CORP.·Product code KOG·August 3, 2011
OPUS SMARTSTITCH M-CONNECTOR
FDA Adverse Event
Other
·ARTHROCARE CORP.·Product code KOG·August 3, 2011
OPUS SMARTSTITCH SUTURE CARTRIDGE
FDA Adverse Event
Other
·ARTHROCARE CORPORATION·Product code KOG·August 3, 2011
MODIFICATION TO: STRYKER NAVIGATION SYSTEM, STRYKER FLUOROSCOPY SYSTEM,VIRTUAL FLUOROSCOPY
FDA 510(k)
FDA Class 2
·Neurology
INFUSOR SV, INFUSOR LV, BAXTER PAIN MANAGEMENT SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
FIRSTPASS NEEDLE AND SUTURE CAPTURE
FDA Adverse Event
Malfunction
·ARTHROCARE CORP.·Product code LXH·October 21, 2011
FIRSTPASS SUTURE PASSER
FDA Adverse Event
Malfunction
·ARTHROCARE CORP.·Product code HWQ·October 21, 2011
FIRSTPASS NEEDLE AND SUTURE CAPTURE
FDA Adverse Event
Malfunction
·ARTHROCARE CORP.·Product code LXH·October 21, 2011
FIRSTPASS NEEDLE AND SUTURE CAPTURE
FDA Adverse Event
Malfunction
·ARTHROCARE CORP.·Product code LXH·October 21, 2011