24 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Universa Soft Ureteral Stents and Stent Sets
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
UNIVERSA SOFT URETERAL STENT SET
FDA Adverse Event
Malfunction
·COOK INC·Product code FAD·January 29, 2019
UNIVERSA SOFT URETERAL STENT SET
FDA Adverse Event
Malfunction
·COOK UROLOGICAL INC·Product code FAD·May 13, 2016
UNIVERSA SOFT URETERAL STENT SET
FDA Adverse Event
Injury
·COOK INC·Product code FAD·September 8, 2016
UNIVERSA SOFT URETERAL STENT SET
FDA Adverse Event
Injury
·COOK UROLOGICAL INC·Product code FAD·May 13, 2016
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code FAD·July 23, 2019
AGXO
FDA UDI
Oticon A/S·05707131282972·H110V2, BTE 13 WL 100 TC AGXO
MAKOPLASTY
FDA UDI
MAKO SURGICAL CORP.·00848486029630·CASE, MICS HANDPIECE & KNEE ATTACHMENT KIT
AGC TRADITION KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304240698·
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100165·KRATZ-BARRAQUER SPECULUM SMALL
RAPIDFLAP SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00841036077709·
Procera®
FDA UDI
Nobel Biocare AB·07332747069716·PROCERA IMPLANT BRIDGE FULL ARCH ABU LEV
Rumex
FDA UDI
RUMEX INTERNATIONAL CORP.·00840159907511·Viscocanalostomy Cannula, 30 Ga, 5.00 mm Bevele...
AVS A-LAT PEEK SPACERS, MODELS 48750XXX, 48751XXX, 48752XXX, 48753XXX
FDA 510(k)
FDA Class 2
·Orthopedic
CONCIERGE GUIDING CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
PROCERA IMPLANT BRIDGE, MODELS 15-1001, 15-1002, 15-1051, 15-1052
FDA 510(k)
FDA Class 2
·Dental
PROCERA IMPLANT BRIDGE, MODELS 15-1001, 15-1002, 15-1051, 15-1052
FDA 510(k)
FDA Class 2
·Dental
PHILIP CPAP DEVICE
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 2, 2025
IDENTITY XL DR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC. CRMD·Product code DXY·January 13, 2014
ASR UNI FEMORAL IMPL SIZE 46
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·June 6, 2013