EBI PATIENT CARE, INC.

FDA Device Registration & Listing · GUAYNABO, PR, US · Registration 3003435252

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3003435252
FEI Number
3003435252
Entity Name
EBI PATIENT CARE, INC.
City/State/Country
GUAYNABO, PR, US
Establishment Address
484 Calle E, GUAYNABO, PR 00969, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
EBI, LLC - AHP EOS Buyer Inc. (Owner Number: 2242816)
Owner / Operator Contact Address
1 Gatehall Drive, Suite 303, Parsippany, NJ 07054, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
P790005

All Registered Proprietary Names

SpinalPak II Bone Growth Stimulator OrthoPak 2 Bone Growth Stimulator S Biomet OrthoPak Non-invasive Bone Growth Stimulator System Biomet Spinalpak Non-invasive Spine Fusion Stimulator System EBI Bone Healing System Biomet EBI Bone Healing System Biomet BHS Mini EBI Bone Healing System-Model 2100 EBI Osteogen Implantable Growth Sti

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LOF Stimulator, Bone Growth, Non-Invasive Orthopedic Class 2 890.5870 2008-02-27
LOF Stimulator, Bone Growth, Non-Invasive Orthopedic Class 2 890.5870 2008-02-27
LOE Stimulator, Invasive Bone Growth Unknown Class 3 N/A 2008-02-27

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

EBI, LLC - AHP EOS Buyer Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
2242816 EBI, LLC PARSIPPANY, NJ, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003435252. Last updated year: 2026. Please use registration number 3003435252 when referencing this establishment in official correspondence.
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