Data / Medical devices / Lamp, Infrared, Therapeutic Heating / United Kingdom
FDA-registered makers of Lamp, Infrared, Therapeutic Heating in the United Kingdom: 9 establishments
9 establishments in the United Kingdom are registered with the FDA to make Lamp, Infrared, Therapeutic Heating (product code ILY). 5 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Lamp, Infrared, Therapeutic Heating
- Product code
- ILY
- Country
- United Kingdom
Makers of Lamp, Infrared, Therapeutic Heating in the United Kingdom
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Aesthetic Technology Ltd | Warrington Cheshire East, United Kingdom | Manufacturer | 1 | December 16, 2020 | 0 | 0 | 0 | api.fda.gov |
| Assembly Contracts Ltd | Manchester Lancashire, United Kingdom | Contract manufacturer, Manufacturer | 1 | March 15, 2005 | 0 | 0 | 0 | api.fda.gov |
| TFT Electronics Ltd | Skeld Shetland Islands, United Kingdom | Contract manufacturer, Specification developer | 1 | March 21, 2006 | 0 | 0 | 0 | api.fda.gov |
| THOR Photomedicine Ltd | Amersham Buckinghamshire, United Kingdom | Manufacturer, Specification developer | 1 | March 17, 2004 | 0 | 3 | 0 | api.fda.gov |
| The Beauty Tech Group Ltd | Macclesfield Cheshire East, United Kingdom | Exporter to the US, Specification developer | 1 | March 9, 2023 | 0 | 0 | 0 | api.fda.gov |
| I-SMART Development LTD. | Sutton Coldfield Birmingham, United Kingdom | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Key-Tech Scotland Ltd | Dunfermline Fife, United Kingdom | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lyma Life Ltd. | London London, City of, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Opatra Ltd | London London, City of, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.