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180 INNOVATIONS LLC

US

Last updated May 24, 2026

What 180 INNOVATIONS LLC makes

180 Innovations LLC manufactures disposable and reusable electronic thermometer probe covers, as well as intermittent and infrared ear-based patient thermometers designed for clinical and retail use. These devices are intended for accurate body temperature measurement in various settings, including hospitals, pharmacies, and home care environments.

The company’s products are classified as Class II medical devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. These devices are intended for distribution in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does 180 Innovations LLC manufacture?

180 Innovations LLC produces electronic thermometers, including intermittent electronic patient thermometers and infrared ear-based thermometers. They also manufacture disposable and reusable electronic thermometer probe covers. These devices are designed for clinical and retail use to measure body temperature accurately in settings like hospitals, pharmacies, and home care.

Where is 180 Innovations LLC based?

180 Innovations LLC is based in the United States. The company’s devices are specifically intended for distribution within the US market.

Which regulatory registries or databases list 180 Innovations LLC’s devices?

180 Innovations LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorised for use in the United States.

How are the devices manufactured by 180 Innovations LLC classified under FDA regulations?

The devices produced by 180 Innovations LLC fall under the classification of Class II medical devices according to FDA regulations. Class II devices generally pose moderate risk and require special controls to ensure their safety and effectiveness, such as performance standards or post-market surveillance.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
(303) 271-0300
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
126646582

Catalogue (34)

DeviceModel / ReferenceRegistriesClassStatus
Rite Aid KD-1540.RA
FDA UDI
Class IIActive
Rite Aid KD-1780FFB.RA
FDA UDI
Class IIActive
Rite Aid KI-8130.RA
FDA UDI
Class IIActive
Bestmed KD-1631.BM
FDA UDI
Class IIActive
Bestmed KD-2160.BM
FDA UDI
Class IIActive
Bestmed KD-113.BM
FDA UDI
Class IIActive
Rite Aid KD-2201L.RA
FDA UDI
Class IIUnknown
Rite Aid KI-8271.RA
FDA UDI
Class IIActive
Bestmed KI-8170.BM
FDA UDI
Class IIActive
Bestmed KD-135.BM
FDA UDI
Class IIActive
Rite Aid 740.RA
FDA UDI
Class IIUnknown
Rite Aid KD-1780Baby.RA
FDA UDI
Class IIActive
Bestmed KD-2050.BM
FDA UDI
Class IIActive
Rite Aid KD-2090.RA
FDA UDI
Class IIUnknown
Rite Aid K-955.RA
FDA UDI
Class IIActive
Rite Aid KD-2250.RA
FDA UDI
Class IIActive
Rite Aid KI-8170L.RA
FDA UDI
Class IIUnknown
Rite Aid KD-2050.RA
FDA UDI
Class IIUnknown
Bestmed KD-192.BM
FDA UDI
Class IIActive
Rite Aid KD-235.RA
FDA UDI
Class IIUnknown
Bestmed KD-118.BM
FDA UDI
Class IIActive
Rite Aid KD-2090BABY.RA
FDA UDI
Class IIUnknown
Rite Aid KD-1780-1.RA
FDA UDI
Class IIActive
Rite Aid KI-8160.RA
FDA UDI
Class IIUnknown
Polygreen KI-8280
FDA UDI
Class IIActive
Rite Aid KD-113.RA
FDA UDI
Class IIUnknown
Bestmed K-953.BM
FDA UDI
Class IIActive
Bestmed KD-133.BM
FDA UDI
Class IIActive
Bestmed DTT-1.BM
FDA UDI
Class IIActive
Bestmed HTD8813C
FDA UDI
Class IIActive
Rite Aid KD-2050baby.RA
FDA UDI
Class IIUnknown
Rite Aid KD-2280.RA
FDA UDI
Class IIActive
Rite Aid KD-133baby.RA
FDA UDI
Class IIUnknown
Rite Aid KD-1780FF.RA
FDA UDI
Class IIActive

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