Data / Medical devices / United Kingdom / TFT Electronics Ltd
TFT Electronics Ltd: FDA-registered device maker in Skeld Shetland Islands, United Kingdom, 1 510(k) clearance
TFT Electronics Ltd is registered with the FDA (registration 3006849751) in Skeld Shetland Islands, United Kingdom. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 21, 2006. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3006849751
- Address
- Unit 1 Skeld Industrial Estate, Skeld Shetland Islands, United Kingdom, ZE2 9NL
- Owner or operator
- TFT Electronics (10030304)
- Roles
- Contract manufacturer, Specification developer
- First device listed
- September 11, 2009
- Registered through
- 2026
- Brand names listed
- Apollo, LZR7
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Contract manufacturer, Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 21, 2006 | K060134 | APOLLO IR HEAT LAMP SYSTEM | ILY | Substantially Equivalent | Apollo Physical Therapy Products International | accessdata.fda.gov |
Compare with other makers
Updated March 21, 2006. 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.