Data / Medical devices / United Kingdom / Design Specific Ltd
Design Specific Ltd: FDA-registered device maker in Laughton East Sussex, United Kingdom, 1 510(k) clearance
Design Specific Ltd is registered with the FDA (registration 3008457027) in Laughton East Sussex, United Kingdom. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 23, 2010. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008457027
- Address
- Units 1-5 Parkside Shortgate Lane, Laughton East Sussex, United Kingdom, BN8 6DG
- Owner or operator
- Design Specific Ltd (10033728)
- Roles
- Manufacturer
- First device listed
- April 13, 2011
- Registered through
- 2026
- Brand names listed
- 'Comfort' Transport and Treatment Chair, Bariatric Treatment chair, Compact Wheelchair Platform
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Chair, Examination And Treatment | FRK | 1 | Manufacturer | accessdata.fda.gov |
| Chair, Positioning, Electric | INO | 2 | Manufacturer | accessdata.fda.gov |
| Device, Patient Transfer, Powered | FRZ | 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 |
|---|---|---|---|---|---|---|
| December 23, 2010 | K101723 | COMPACT WHEELCHAIR PLATFORM | INO | Substantially Equivalent | Design Specific Fletcher | accessdata.fda.gov |
Compare with other makers
- All makers of Chair, Positioning, Electric
- All makers of Device, Patient Transfer, Powered
- All makers of Chair, Examination And Treatment
Updated December 23, 2010. 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.