GIVMOHR CORPORATION

FDA Device Registration & Listing · Albuquerque, NM, US · Registration 3009832762

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
3009832762
FEI Number
3009832762
Entity Name
GIVMOHR CORPORATION
City/State/Country
Albuquerque, NM, US
Establishment Address
222B Cynthia Loop NW, Albuquerque, NM 87114, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
GivMohr Corporation (Owner Number: 10042059)
Owner / Operator Contact Address
222B Cynthia Loop NW, Albuquerque, NM 87114, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

GivMohr Sling

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ILI Sling, Arm Physical Medicine Class 1 890.3640 2012-10-12

Official Correspondent

Paul Mohr

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

GivMohr Corporation
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009832762. Last updated year: 2026. Please use registration number 3009832762 when referencing this establishment in official correspondence.
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