Navajo Manufacturing Company Inc.
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.
Catalogue
Search and filter all 429 devicesShowing 1-50 of 429
Company details
- FDA FEI number
- 1000065475
- Address
- 5330 FOX ST., Denver, CO, 80216
FDA recalls
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.
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.
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.