G-FORCE BRACES

FDA Device Registration & Listing · Manchester, NH, US · Registration 3007222848

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
3007222848
FEI Number
3007222848
Entity Name
G-FORCE BRACES
City/State/Country
Manchester, NH, US
Establishment Address
140 March Ave, Manchester, NH 03103, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
G-Force Braces (Owner Number: 10033579)
Owner / Operator Contact Address
140 March Ave, Manchester, NH 03103, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Cryo Pack Sleeper Brace Shoulder Pneumatic Cryo Compression Device Knee Pneumatic Cryo Compression Device Cryo Back Brace

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IME Pack, Hot Or Cold, Reusable Physical Medicine Class 1 890.5700 2013-06-13
IQI Orthosis, Limb Brace Physical Medicine Class 1 890.3475 2010-09-01
IPY Orthosis, Lumbo-Sacral Physical Medicine Class 1 890.3490 2018-04-02

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

G-Force Braces
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 3007222848. Last updated year: 2026. Please use registration number 3007222848 when referencing this establishment in official correspondence.
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