FDA.reportPublic FDA data

EBI, LLC

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
22428162242816EBI, LLC1N2026-01-011 Gatehall Rd. Suite 303 PARSIPPANY NJ US 07054

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00880304820852Biomet SpinalPak / OrthoPak - ELECTRODES, 63B, SPINALPAK/ORTHOPAK1.973.299.9300btbs.csorders@biomet.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
362691604711620P850035SpF® Implantable Spinal Fusion StimulatorLOE1987-04-30
362691343828957P850022Biomet® OrthoPak® Non-invasive Bone Growth Stimulator System; Biomet® SpinalPak® Non-invasive Spine Fusion Stimulator SyLOF1986-02-18
362691370116180P790005OsteoGenTM Implantable Bone Growth StimulatorsLOE1980-01-25
362691987108320P790002Biomet(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

PMA#

165 records. Showing 1-40. Next

PMN#

GUDID#

77 records. Showing 1-40. Next