10 results
·
27ms
·
Sources: EU EUDAMED, US FDA
VERO CELLS
FDA 510(k)
FDA Class 1
·Hematology
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704261493·
DANMAR PRODUCTS, INC.
FDA registration
DANMAR PRODUCTS, INC.·4 products·🇺🇸 United States
AccelFix Lumbar Expandable Cage System
FDA 510(k)
FDA Class 2
·Orthopedic
SPECTRAPULSE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ADULT DUAL HEATED EVAQUA2 BREATHING CIRCUIT
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BZE·May 26, 2014
OCTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·November 9, 2012
HARMONIC ACE 23 CM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code LFL·September 12, 2007
ACCOLADE SR SL MRI (Model L310)
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·October 22, 2025
Allura Xper FD20; Catalog numbers: (1) 722006, (2) 722012, (3) 722028.
FDA Enforcement
Class I
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 26, 2025