Data / Medical devices / United Kingdom / Flexible Medical Packaging Ltd.
Flexible Medical Packaging Ltd.: FDA-registered device maker in LANCASTER Lancashire, United Kingdom, 3 510(k) clearances
Flexible Medical Packaging Ltd. is registered with the FDA (registration 3004512585) in LANCASTER Lancashire, United Kingdom. It lists 7 device types. The FDA files 3 510(k) clearances under its listings, the newest dated August 10, 2010. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004512585
- Address
- Unit 8, Hightown Whitecross Industrial Estate, LANCASTER Lancashire, United Kingdom, LA1 4XS
- Owner or operator
- Flexible Medical Packaging Ltd (9035506)
- Roles
- Contract manufacturer, Manufacturer, Repackager or relabeler
- First device listed
- December 22, 2006
- Registered through
- 2026
- Brand names listed
- Liberty Soft Skin Adhesive remover, Liberty Soft Skin Barrier Flim, Opticell, Opticell Ag, Optifoam, WELLAND ADHESIVE REMOVER, WELLAND BARRIER FILM
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bandage, Liquid | KMF | 1 | Contract manufacturer | accessdata.fda.gov |
| Bandage, Liquid, Skin Protectant | NEC | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Dressing, Wound, Drug | FRO | U | Repackager or relabeler | accessdata.fda.gov |
| Dressing, Wound, Hydrophilic | NAC | 1 | Manufacturer | accessdata.fda.gov |
| Dressing, Wound, Occlusive | NAD | 1 | Manufacturer | accessdata.fda.gov |
| Hemostatic Wound Dressing Without Thrombin Or Other Biologics | QSY | U | Repackager or relabeler | accessdata.fda.gov |
| Solvent, Adhesive Tape | KOX | 1 | Contract 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 |
|---|---|---|---|---|---|---|
| August 10, 2010 | K100693 | AQUANOVA AG SUPER ABSORBANT DRESSING, AQUANOVA AG ANTIMICROBIAL DRESSING | FRO | Substantially Equivalent | Medtrade Products Limited | accessdata.fda.gov |
| July 25, 2007 | K070175 | AQUANOVA SUPER-ABSORBENT GELLING DRESSING, OTC | QSY | Substantially Equivalent | Medtrade Products , Ltd. | accessdata.fda.gov |
| December 1, 2004 | K033732 | MEDTRADE PRODUCTS ANTISEPTIC BARRIER SILVER FOAM DRESSING, MODEL 09912450 | FRO | Substantially Equivalent | Medtrade Products , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Dressing, Wound, Occlusive
- All makers of Bandage, Liquid
- All makers of Dressing, Wound, Hydrophilic
- All makers of Hemostatic Wound Dressing Without Thrombin Or Other Biologics
- All makers of Bandage, Liquid, Skin Protectant
- All makers of Dressing, Wound, Drug
Updated August 10, 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.