3FDM, INC.

FDA Device Registration & Listing · Largo, FL, US · Registration 3021187078

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
3021187078
FEI Number
3021187078
Entity Name
3FDM, INC.
City/State/Country
Largo, FL, US
Establishment Address
10600 Endeavour Way, Largo, FL 33777, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
3FDM, Inc. (Owner Number: 10083458)
Owner / Operator Contact Address
10600 Endeavour Way, Largo, FL 33777, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

STRETCHER, HAND-CARRIED TOURNIQUET, NONPNEUMATIC

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FPP Stretcher, Hand-Carried General Hospital Class 1 880.6900 2021-11-22
GAX Tourniquet, Nonpneumatic General, Plastic Surgery Class 1 878.5900 2021-11-22

Official Correspondent

Babu Parvataneni

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

3FDM, Inc.
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 3021187078. Last updated year: 2026. Please use registration number 3021187078 when referencing this establishment in official correspondence.
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