Data / Medical devices / United Kingdom / Meditech Endoscopy Ltd
Meditech Endoscopy Ltd: FDA-registered device maker in Basildon Essex, United Kingdom, 1 510(k) clearance
Meditech Endoscopy Ltd is registered with the FDA (registration 3011346938) in Basildon Essex, United Kingdom. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 7, 2019. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011346938
- Address
- Suite 1 Bowden Terminal Luckyn Lane, Basildon Essex, United Kingdom, SS14 3AX
- Owner or operator
- Meditech Endoscopy Ltd (10049602)
- Roles
- Manufacturer
- First device listed
- June 26, 2015
- Registered through
- 2026
- Brand names listed
- Clean Cage, Clean Tray, PrioriTag, Protech, StageOne Enzymatic, StageOne Neutral, ToteTimer, Valve Safe
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Adaptor, Bulbs, Miscellaneous, For Endoscope | FFY | 1 | Manufacturer | accessdata.fda.gov |
| Basin For Endoscope Reprocessing | PHT | 1 | Manufacturer | accessdata.fda.gov |
| Endoscopic Storage Cover | OCU | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| May 7, 2019 | K191011 | Scope ProTech | OCU | Substantially Equivalent | Meditech Endoscopy, Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Endoscopic Storage Cover
- All makers of Adaptor, Bulbs, Miscellaneous, For Endoscope
- All makers of Basin For Endoscope Reprocessing
Updated May 7, 2019. 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.