Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1320537

FEI Number

3000215374

Entity Name

FIELDTEX PRODUCTS, INC.

City/State/Country

ROCHESTER, NY, US

Establishment Address

2921 BRIGHTON-HENRIETTA TL RD., ROCHESTER, NY 14623, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

FIELDTEX PRODUCTS, INC. (Owner Number: 9027566)

Owner / Operator Contact Address

2921 BRIGHTON-HENRIETTA TL RD., --, Rochester, NY 14623, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Fieldtex Fieldtex

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OHO	First Aid Kit Without Drug	General, Plastic Surgery	Class 1	878.4014	2010-07-09
LRR	First Aid Kit With Drug	Unknown	Class N	N/A	2010-07-09

Official Correspondent

Jon Abbey

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

FIELDTEX PRODUCTS, 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 1320537. Last updated year: 2026. Please use registration number 1320537 when referencing this establishment in official correspondence.