Data / Medical devices / United Kingdom / Lantor (uk), Ltd.
Lantor (uk), Ltd.: FDA-registered device maker in BOLTON North Yorkshire, United Kingdom, 1 510(k) clearance
Lantor (uk), Ltd. is registered with the FDA (registration 8021899) in BOLTON North Yorkshire, United Kingdom. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 6, 1988. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 8021899
- FEI number
- 6664
- Address
- Sunnyside Business Centre Adeline Street, BOLTON North Yorkshire, United Kingdom, BL3 3NY
- Owner or operator
- LANTOR (UK), LTD. (8021899)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- April 10, 2006
- Registered through
- 2026
- Brand names listed
- BANDAGE, CAST, Indicator, physical/chemical sterilization process, PROFORE WCL
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bandage, Cast | ITG | 1 | Contract manufacturer | accessdata.fda.gov |
| Gauze / Sponge,Nonresorbable For External Use | NAB | 1 | Contract manufacturer | accessdata.fda.gov |
| Indicator, Physical/Chemical Sterilization Process | JOJ | 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 |
|---|---|---|---|---|---|---|
| October 6, 1988 | K882756 | LANTOR CUBE STERILIZER TEST PACK | JOJ | Substantially Equivalent | Lantor Group | accessdata.fda.gov |
Compare with other makers
- All makers of Gauze / Sponge,Nonresorbable For External Use
- All makers of Bandage, Cast
- All makers of Indicator, Physical/Chemical Sterilization Process
Updated October 6, 1988. 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.