FDA.reportPublic FDA data

EBI PATIENT CARE, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30034352523003435252EBI PATIENT CARE, INC.1Y2026-01-01484 Calle E GUAYNABO PR US 00969

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
362721604711620P850035SpF® Implantable Spinal Fusion StimulatorLOE1987-04-30
362721343828957P850022Biomet® OrthoPak® Non-invasive Bone Growth Stimulator System; Biomet® SpinalPak® Non-invasive Spine Fusion Stimulator SyLOF1986-02-18
362721370116180P790005OsteoGenTM Implantable Bone Growth StimulatorsLOE1980-01-25
362721987108320P790002Biomet(R) EBI BONE Healing SystemLOF1979-11-06

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
LOE21987-04-30
LOF21986-02-18