Limber Prosthetics, Inc.

FDA Device Registration & Listing · San Diego, CA, US · Registration 3030088168

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
3030088168
FEI Number
3030088168
Entity Name
Limber Prosthetics, Inc.
City/State/Country
San Diego, CA, US
Establishment Address
4883 Ronson Ct Ste G, San Diego, CA 92111, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
Limber Prosthetics, Inc. (Owner Number: 10089479)
Owner / Operator Contact Address
4883 Ronson Ct., STE G, San Diego, CA 92111, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

UniLeg Limber Foot 1 LF1 Limber LF1 Limber Foot One

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KFX Assembly, Thigh/Knee/Shank/Ankle/Foot, External Physical Medicine Class 2 890.3500 2023-12-11
ISH Component, External, Limb, Ankle/Foot Physical Medicine Class 1 890.3420 2026-02-05

Official Correspondent

Joshua Pelz

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Limber Prosthetics, Inc.
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 3030088168. Last updated year: 2026. Please use registration number 3030088168 when referencing this establishment in official correspondence.
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