66 results
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23ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Stryker ICONIX with Needles
FDA 510(k)
FDA Class 2
·Orthopedic
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772813148·GENUMEDI PRO SILVER SIZE I
ResinBlend LV Composite Blending Resin
FDA UDI
DEN-MAT HOLDINGS, LLC·00359883003791·Dental unfilled resin sealant/coating
Oticon
FDA UDI
Oticon A/S·05707131280251·H11, DESIGNRITE 10 WL CRED
ResinBlend LV Composite Blending Resin
FDA UDI
CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172017084·Dental unfilled resin sealant/coating
STRYKER
FDA UDI
MAKO SURGICAL CORP.·07613327409086·MAKO KNEE TRAY BASE
Brasseler USA
FDA UDI
Peter Brasseler Holdings, LLC·00887919890218·RESINBLEND LV 3ML/BOTTLE 1P
General Instruments
FDA UDI
ALPHATEC SPINE, INC.·00840180526132·A-ARM ADAPTOR, M-TUBE, LTP
LEONE SPA
FDA UDI
LEONE SPA·08033707071495·MINI ORTHODONTIC IMPLANT LOW D1,5 L12 mm
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575289769·Orthopaedic implant aiming/guiding block, reusa...
n/a
FDA UDI
Ortho Development Corporation·00822409070459·Snap-on Fem Augment Trial 12mm Distal Size 5
E1 MEDICAL FLAT PANEL DISPLAY SYSTEM AND MFGD 1218 MEDICAL FLAT PANEL DISPLAY
FDA 510(k)
FDA Class 2
·Radiology
STRAIGHT ABUTMENT, 4.2, 4.6, 5.0, 6.4, IMPLANT 6.0, IMPLANT 7.0, IMPLANT 8.0 MODEL: 002061, 002062, 002063, 002064,
FDA 510(k)
FDA Class 2
·Dental
BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAVED KIT
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·April 12, 2024
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2013
COGNIS
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·July 6, 2011
DAMON COPPER NITI WIRE
FDA Adverse Event
Malfunction
·ORMCO CORPORATION·Product code DZC·September 9, 2008
SPECTRANETICS QUICK-CROSS SUPPORT CATHETER
FDA Adverse Event
Injury
·THE SPECTRANETICS CORPORATION·Product code DQY·March 6, 2019
BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·September 3, 2025
BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·September 3, 2025