Data / Medical devices / Powered Laser Surgical Instrument / United Kingdom
FDA-registered makers of Powered Laser Surgical Instrument in the United Kingdom: 8 establishments
8 establishments in the United Kingdom are registered with the FDA to make Powered Laser Surgical Instrument (product code GEX). 7 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Powered Laser Surgical Instrument
- Product code
- GEX
- Country
- United Kingdom
Makers of Powered Laser Surgical Instrument 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 | 2 | June 4, 2024 | 0 | 0 | 0 | api.fda.gov |
| Assembly Contracts Ltd | Manchester Lancashire, United Kingdom | Contract manufacturer, Manufacturer | 2 | July 17, 2003 | 0 | 0 | 0 | api.fda.gov |
| Cyden Limited | Swansea, Wales, United Kingdom | Complaint file establishment, Specification developer | 1 | May 8, 2017 | 0 | 0 | 0 | api.fda.gov |
| Keeler Ltd. | WINDSOR, BERKSHIRE Windsor and Maidenhead, United Kingdom | Manufacturer | 1 | February 28, 2017 | 0 | 0 | 0 | api.fda.gov |
| Lustre Skin Ltd | Livingston Scotland, United Kingdom | Specification developer | 1 | January 19, 2016 | 0 | 0 | 0 | api.fda.gov |
| Moor Instruments Ltd. | AXMINSTER Devon, United Kingdom | Manufacturer | 1 | January 13, 2009 | 0 | 0 | 0 | api.fda.gov |
| The Beauty Tech Group Ltd | Macclesfield Cheshire East, United Kingdom | Exporter to the US, Specification developer | 1 | December 23, 2009 | 0 | 0 | 0 | api.fda.gov |
| CYDEN Ltd | Swansea, United Kingdom | Exporter to the US, Manufacturer, Repackager or relabeler | 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.