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Navajo Manufacturing Company Inc.

Also registered as NAVAJO MANUFACTURING COMPANY

United Statesfrom the FDA registration address FDA establishment FEI 1000065475

Devices
429
Registrations
FDA
FDA recalls
11 ongoing

What Navajo Manufacturing Company Inc. makes

Navajo Manufacturing Company Inc. produces tinted non-prescription spectacles, magnifying spectacles, unscented menstrual tampons, compression gloves, medicated first aid kits, intermittent electronic thermometers, dental floss dispensers, and dental floss.

The company’s portfolio includes devices classified as Class I, Class II, and non-classified (N), all listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue429

Newest first, rows 1-50 of 429

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  • Withdrawn Registry: GUDID Class:II
  • Handy Solutions 25756

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Handy Solutions 31232 Open recall

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Piranha 87373

    Listed Registry: GUDID Class:I
  • Piranha 87228

    Listed Registry: GUDID Class:I
  • Piranha 62126

    Listed Registry: GUDID Class:I
  • Piranha 62026

    Listed Registry: GUDID Class:I
  • Piranha 87268

    Listed Registry: GUDID Class:I
  • Maxx 57598

    Listed Registry: GUDID Class:I
  • Piranha 59691

    Listed Registry: GUDID Class:I
  • Maxx 57576

    Listed Registry: GUDID Class:I
  • Piranha 87317

    Listed Registry: GUDID Class:I
  • Piranha 60059

    Listed Registry: GUDID Class:I
  • Piranha 62183

    Listed Registry: GUDID Class:I
  • Piranha 60099

    Listed Registry: GUDID Class:I
  • Piranha 62117

    Listed Registry: GUDID Class:I
  • Piranha 90001

    Listed Registry: GUDID Class:I
  • Handy Solutions 26101

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Piranha 62011

    Listed Registry: GUDID Class:I
  • Maxx 57588

    Listed Registry: GUDID Class:I
  • Piranha 87342

    Listed Registry: GUDID Class:I
  • Piranha 87325

    Listed Registry: GUDID Class:I
  • Piranha 62076

    Listed Registry: GUDID Class:I
  • Piranha 62046

    Listed Registry: GUDID Class:I
  • Piranha 52912

    Listed Registry: GUDID Class:I
  • Maxx 57241

    Listed Registry: GUDID Class:I
  • Piranha 87219

    Listed Registry: GUDID Class:I
  • Maxx 57613

    Listed Registry: GUDID Class:I
  • Piranha 52941

    Listed Registry: GUDID Class:I
  • Piranha 60067

    Listed Registry: GUDID Class:I
  • Piranha 87273

    Listed Registry: GUDID Class:I
  • Handy Solutions 28141

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Piranha 62190

    Listed Registry: GUDID Class:I
  • Piranha 59839

    Listed Registry: GUDID Class:I
  • Piranha 62151

    Listed Registry: GUDID Class:I
  • Piranha 62062

    Listed Registry: GUDID Class:I
  • Piranha 62123

    Listed Registry: GUDID Class:I
  • Piranha 87263

    Listed Registry: GUDID Class:I
  • Piranha 62105

    Listed Registry: GUDID Class:I
  • Piranha 90009

    Listed Registry: GUDID Class:I
  • Piranha 62161

    Listed Registry: GUDID Class:I
  • Piranha 80297

    Listed Registry: GUDID Class:I
  • Piranha 60114

    Listed Registry: GUDID Class:I
  • Piranha 87227

    Listed Registry: GUDID Class:I
  • Oral Care 29067

    Listed Registry: GUDID Class:I
  • Piranha 62177

    Listed Registry: GUDID Class:I
  • Piranha 62103

    Listed Registry: GUDID Class:I
  • Piranha 87395

    Listed Registry: GUDID Class:I
  • Handy Solutions 26101

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Piranha 60142

    Listed Registry: GUDID Class:I

Rows 1-50 of 429

Showing 1-50 of 429

Company details

FDA FEI number
1000065475
Address
5330 FOX ST., Denver, CO, 80216

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 1 Nov 2026.

FDA recall records list 1 recall initiated by Navajo Manufacturing Company Inc., initiated on 2026-02-18. By recorded status: 1 ongoing. The reasons filed fall into these groups: electrical or power. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

Recalls initiated per year

  • 2017 0
  • 2018 0
  • 2019 0
  • 2020 0
  • 2021 0
  • 2022 0
  • 2023 0
  • 2024 0
  • 2025 0
  • 2026 1
  • 2026

    • 18 Feb 2026 Z-1588-2026 Class I Ongoing If heating pad is folded while in use, the power density increases in the folded area causing excessive temperatures, which can also be caused by placing pad under the body, then the high limit device is unable to sense the higher temperature so power is not terminated. May cause a burning smell prior to melting/burning potentially causing burns to persons and property. Distribution: US Nationwide distribution in the states of CA, MS, FL, IN, LA, VA, TX.

Frequently asked questions

How many devices does Navajo Manufacturing Company Inc. have in the registry?

The registry currently lists 429 devices for Navajo Manufacturing Company Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Navajo Manufacturing Company Inc.'s devices?

Among its 50 most recently registered devices, Navajo Manufacturing Company Inc. has devices listed in FDA GUDID (50 devices).

What risk classes do Navajo Manufacturing Company Inc.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for Navajo Manufacturing Company Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for Navajo Manufacturing Company Inc.?

FDA recall records list 1 recall initiated by Navajo Manufacturing Company Inc., the most recent initiated on 18 Feb 2026. 1 of them is recorded as ongoing. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from Navajo Manufacturing Company Inc. in the registry?

The most recently registered devices listed for Navajo Manufacturing Company Inc. include HANDY SOLUTIONS HEATING PAD WRAP SHOULDER AND NECK 25607, Handy Solutions 25756, Handy Solutions 31232 and Piranha 87373.

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company.