Data / Medical devices / United Kingdom / Davis Schottlander & Davis, Ltd.
Davis Schottlander & Davis, Ltd.: FDA-registered device maker in LETCHWORTH, HERTS. Hertfordshire, United Kingdom, 3 510(k) clearances
Davis Schottlander & Davis, Ltd. is registered with the FDA (registration 9681531) in LETCHWORTH, HERTS. Hertfordshire, United Kingdom. It lists 3 device types. The FDA files 3 510(k) clearances under its listings, the newest dated August 25, 2003. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9681531
- FEI number
- 1000269600
- Address
- Fifth Ave. Letchworth Garden City, LETCHWORTH, HERTS. Hertfordshire, United Kingdom, SG6 2WD
- Owner or operator
- DAVIS SCHOTTLANDER & DAVIS, LTD. (9024615)
- Roles
- Exporter to the US, Manufacturer, Repackager or relabeler, Specification developer
- First device listed
- December 10, 2007
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Denture, Plastic, Teeth | ELM | 2 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Powder, Porcelain | EIH | 2 | Exporter to the US, Manufacturer, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Resin, Denture, Relining, Repairing, Rebasing | EBI | 2 | Exporter to the US, Repackager or relabeler, 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 |
|---|---|---|---|---|---|---|
| August 25, 2003 | K024250 | MATCH PRESS PRESSABLE CERAMIC | EIH | Substantially Equivalent | Davis Schottlander & Davis, Ltd. | accessdata.fda.gov |
| December 22, 1999 | K993717 | ENIGMA HI-BASE DENTURE BASE MATERIAL | EBI | Substantially Equivalent | Davis Schottlander & Davis, Ltd. | accessdata.fda.gov |
| February 12, 1999 | K984134 | NATURA DENTURE TEETH | ELM | Substantially Equivalent | Davis Schottlander & Davis, Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Powder, Porcelain
- All makers of Resin, Denture, Relining, Repairing, Rebasing
- All makers of Denture, Plastic, Teeth
Updated August 25, 2003. 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.