10 results
·
41ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
V-PRO maX 2 Low Temperature Sterilization System
FDA 510(k)
FDA Class 2
·General Hospital
NA
FDA UDI
STRYKER CORPORATION·07613327051667·Fiberoptic Light Cable (Wolf Scope and Stryker ...
Lumbar Spine Truss System Plating Solution (LSTS-PS)
FDA 510(k)
FDA Class 2
·Orthopedic
SYNTHES 2.0 MM CRANIOFACIAL LOCKING PLATES
FDA 510(k)
FDA Class 2
·Dental
STERRAD 100S STERILIZER
FDA Adverse Event
Malfunction
·ADVANCED STERILIZATION PRODUCTS·Product code MLR·February 1, 2010
FLO-GARD 6201 VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE (SG)·Product code FRN·November 18, 2008
CURLIN ADMINISTRATION SET
FDA Adverse Event
Malfunction
·MOOG MEDICAL DEVICES GROUP·Product code FRN·July 26, 2011
12/14 ARTICUL 40MM M SPEC+5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·July 18, 2013
CODMAN Disposable Perforator, 14mm. Cranial perforator.
FDA Enforcement
Class I
·Ongoing·Integra LifeSciences Corp. (NeuroSciences)·May 14, 2025
Model Number L111, ESSENTIO DR SL MRI Pacemaker
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·October 22, 2025