Identity
- Trade Name
- Aegis Infrared Thermometer FDA UDI
- Generic Name
- Infrared patient thermometer, skin FDA UDI
- Device Name
- Electronic infrared thermometer for clinical use. FDA UDI
- Model / Reference
- LX-26E FDA UDI
- Description
- Electronic infrared thermometer for clinical use. FDA UDI
Identifiers
- Catalog Number
- 005-00044 FDA UDI
- Primary DI / UDI-DI
- 00872320004941 FDA UDI
- 510(k) Number
- K160816 FDA UDI
- FDA Product Code
- FLL FDA UDI
- GMDN Term
- Infrared patient thermometer, skin FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.2910 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Infrared patient thermometer, skin
Aegis Infrared Thermometer by Cao Group, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Infrared patient thermometer, skin.
- TytoHome — TYTO CARE LTD · Class II
- ALPHAMED — Shenzhen Urion Technology Co., Ltd. · Class II
- Diagnostix™ — American Diagnostic Corporation · Class II
- Famidoc — FAMIDOC USA, INC. · Class II
- Sinocare Non-contact Infrared Thermometer — Alicn Medical Shenzhen, Inc. · Class II
- Famidoc — Famidoc Technology Company Limited · Class II
- DR.TALBOT'S Non-contact Infrared Thermometer — Alicn Medical Shenzhen, Inc. · Class II
- Berrcom — Guangzhou Berrcom Medical Device Co., Ltd · Class II
Cleared under the same submission
K160816 also covers:
- SAFE-MATE — CASE-MATE, INC.
- BEWELL CONNECT MyThermo — Visiomed Group SA
- THERMOFLASH — Visiomed Group SA
- THERMOFLASH — Visiomed Group SA
- THERMOFLASH — Visiomed Group SA
- THERMOFLASH — Visiomed Group SA
- THERMOFLASH — Visiomed Group SA
- THERMOFLASH — Visiomed Group SA
- THERMOFLASH — Visiomed Group SA
- THERMOFLASH — Visiomed Group SA
- THERMOFLASH — Visiomed Group SA
- THERMOFLASH — Visiomed Group SA
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Cao Group, Inc.
Sources (1)
- FDA UDI 8529aa43-4229-4584-85bf-cff57508d9ee 35 fields · synced May 30, 2026