Data / Medical devices / Negative Pressure Wound Therapy Powered Suction Pump / United Kingdom
FDA-registered makers of Negative Pressure Wound Therapy Powered Suction Pump in the United Kingdom: 7 establishments
7 establishments in the United Kingdom are registered with the FDA to make Negative Pressure Wound Therapy Powered Suction Pump (product code OMP). 3 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.
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- Device
- Negative Pressure Wound Therapy Powered Suction Pump
- Product code
- OMP
- Country
- United Kingdom
Makers of Negative Pressure Wound Therapy Powered Suction Pump in the United Kingdom
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Smith & Nephew Medical Ltd | HULL East Riding of Yorkshire, United Kingdom | Specification developer | 14 | September 11, 2026 | 0 | 2 | 0 | api.fda.gov |
| Talley Group Ltd. | ROMSEY, HANTS. Hampshire, United Kingdom | Complaint file establishment, Manufacturer | 4 | February 19, 2016 | 0 | 0 | 0 | api.fda.gov |
| ConvaTec Limited, GDC Building | Deeside Flintshire, United Kingdom | Specification developer | 2 | June 24, 2026 | 0 | 0 | 0 | api.fda.gov |
| Brightwake Ltd | Kirkby-in-Ashfield Nottinghamshire, United Kingdom | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Meridian Medical Limited | Littlehampton West Sussex, United Kingdom | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Plexus Corp. (UK) Limited | Kelso Scottish Borders, The, United Kingdom | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Systagenix Wound Management Manufacturing Limited | North Yorkshire, United Kingdom | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 2026. 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.