Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012755358

FEI Number

3012755358

Entity Name

MARTIN BIONICS INNOVATIONS, LLC

City/State/Country

Oklahoma City, OK, US

Establishment Address

214 E Main St, Oklahoma City, OK 73104, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Martin Bionics (Owner Number: 10052581)

Owner / Operator Contact Address

214 E MAIN ST, Oklahoma City, OK 73104, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Socket-less Socket Bikini Socket MB Adjust Transfemoral Kit MB Adjust Transtibial Kit

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ISS	Prosthesis, Thigh Socket, External Component	Physical Medicine	Class 1	890.3420	2016-08-19

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Martin Bionics

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012755358. Last updated year: 2026. Please use registration number 3012755358 when referencing this establishment in official correspondence.