Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3031662599

FEI Number

3031662599

Entity Name

SLINGSHOT BIONICS

City/State/Country

Oklahoma City, OK, US

Establishment Address

220 SE 4th St, Suite 400, Oklahoma City, OK 73129, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

SLINGSHOT BIONICS (Owner Number: 10090818)

Owner / Operator Contact Address

220 SE 4th St, Suite 400, okc, OK 73129, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Slingshot Socket

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	2024-06-26

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SLINGSHOT 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 3031662599. Last updated year: 2026. Please use registration number 3031662599 when referencing this establishment in official correspondence.