Data / Medical devices / United Kingdom / Enteral Access Technologies, Ltd.
Enteral Access Technologies, Ltd.: FDA-registered device maker in Caerwys Flintshire, United Kingdom, 1 510(k) clearance
Enteral Access Technologies, Ltd. is registered with the FDA (registration 3025772870) in Caerwys Flintshire, United Kingdom. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated September 30, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3025772870
- Address
- Water Street, Caerwys Flintshire, United Kingdom, CH7 5AT
- Owner or operator
- Enteral Access Technologies, Ltd. (10087023)
- Roles
- Manufacturer
- First device listed
- January 3, 2023
- Registered through
- 2026
- Brand names listed
- DoubleCHEK
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Tubes, Gastrointestinal (And Accessories) | KNT | 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 |
|---|---|---|---|---|---|---|
| September 30, 2022 | K212316 | DoubleChek DC-1001 | KNT | Substantially Equivalent | Nasogastric Feeding Solutions, Ltd. | accessdata.fda.gov |
Compare with other makers
Updated September 30, 2022. 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.