Data / Medical devices / United Kingdom / Network Medical Products, Ltd.
Network Medical Products, Ltd.: FDA-registered device maker in Ripon North Yorkshire, United Kingdom, 2 510(k) clearances
Network Medical Products, Ltd. is registered with the FDA (registration 3001967056) in Ripon North Yorkshire, United Kingdom. It lists 5 device types. The FDA files 2 510(k) clearances under its listings, the newest dated October 29, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3001967056
- Address
- Coronet House, Kearsley Road, Ripon North Yorkshire, United Kingdom, HG4 2SG
- Owner or operator
- NETWORK MEDICAL PRODUCTS, LTD. (9034848)
- Roles
- Manufacturer, Specification developer
- First device listed
- May 26, 2004
- Registered through
- 2026
- Brand names listed
- CORONET Forceps, Cellulose Point, Cellulose Spear, Clear-Vue Recipient Vacuum Trephine for P.K, DALK Clear-Vue Recipient Vacuum Trephine (300 Microns), DMEK Endoglide, DMEK Guarded Trephine Punch, Donor Trephine Punch and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Forceps, Ophthalmic | HNR | 1 | Manufacturer | accessdata.fda.gov |
| Punch, Corneo-Scleral | HNJ | 1 | Manufacturer | accessdata.fda.gov |
| Spatula, Ophthalmic | HND | 1 | Manufacturer | accessdata.fda.gov |
| Sponge, Ophthalmic | HOZ | 2 | Manufacturer, Specification developer | accessdata.fda.gov |
| Trephine, Manual, Ophthalmic | HRH | 1 | 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 29, 2013 | K130117 | NETWORK EYE SPEARS, POINTS, DRAINS, WICKS AND SHIELDS | HOZ | Substantially Equivalent | Network Medical Products, Ltd. | accessdata.fda.gov |
| August 5, 1992 | K920354 | OPHTHALMIC SPONGES | HOZ | Substantially Equivalent | Ultracell Medical Technologies, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Punch, Corneo-Scleral
- All makers of Sponge, Ophthalmic
- All makers of Spatula, Ophthalmic
- All makers of Trephine, Manual, Ophthalmic
- All makers of Forceps, Ophthalmic
Updated October 29, 2013. 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.