Data / Medical devices / United Kingdom / Vernacare Ltd.
Vernacare Ltd.: FDA-registered device maker in Chorley Lancashire, United Kingdom, 1 510(k) clearance
Vernacare Ltd. is registered with the FDA (registration 3015335150) in Chorley Lancashire, United Kingdom. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 4, 2004. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3015335150
- Address
- Vernacare LTD. 1 Western Avenue, Matrix Park, Chorley, PR7 7NB, Chorley Lancashire, United Kingdom, PR7 7NB
- Owner or operator
- Vernacare Ltd (10060165)
- Roles
- Manufacturer
- First device listed
- April 5, 2019
- Registered through
- 2026
- Brand names listed
- ALBERT, BERT, HUBERT, NUBERT
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Laparoscope, General & Plastic Surgery | GCJ | 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 |
|---|---|---|---|---|---|---|
| March 4, 2004 | K033842 | NUBERT, ALBERT AND HUBERT IMPERVIOUS BAGS FOR ENDOSCOPIC RETRIEVAL OF TISSUE | GCJ | Substantially Equivalent | Vernon-Carus Limited | accessdata.fda.gov |
Compare with other makers
Updated March 4, 2004. 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.