Data / Medical devices / United Kingdom / Talley Group Ltd.
Talley Group Ltd.: FDA-registered device maker in ROMSEY, HANTS. Hampshire, United Kingdom, 4 510(k) clearances
Talley Group Ltd. is registered with the FDA (registration 8010348) in ROMSEY, HANTS. Hampshire, United Kingdom. It lists 2 device types. The FDA files 4 510(k) clearances under its listings, the newest dated February 19, 2016. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 8010348
- FEI number
- 1000251124
- Address
- Premier Way, Abbey Park Industrial Estate, ROMSEY, HANTS. Hampshire, United Kingdom, SO51 9AQ
- Owner or operator
- TALLEY GROUP LTD. (8010348)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- February 15, 1978
- Registered through
- 2026
- Brand names listed
- DUO CARE POWER UNIT, NPWT Dressings, TALLEY RIPPLEBED PUMP- PULSAIR PAD, Venturi, Venturi MiNO TG600/14, Venturi NPWT v.11 Advanced vacuum system
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Mattress, Air Flotation, Alternating Pressure | FNM | 2 | Manufacturer | accessdata.fda.gov |
| Negative Pressure Wound Therapy Powered Suction Pump | OMP | 2 | Complaint file establishment, 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 |
|---|---|---|---|---|---|---|
| February 19, 2016 | K151263 | Venturi Gauze Wound Care Sets with Portal Drain | OMP | Substantially Equivalent | Talley Group, Ltd. | accessdata.fda.gov |
| January 5, 2016 | K143004 | VENTURI MiNO TG600/14 | OMP | Substantially Equivalent | Talley Group, Ltd. | accessdata.fda.gov |
| August 25, 2009 | K090258 | VENTURI NPWT V. II ADVANCED VACUUM SYSTEM | OMP | Substantially Equivalent | Talley Medical | accessdata.fda.gov |
| July 15, 2008 | K080897 | VENTURI NEGATIVE PRESSURE WOUND THERAPY SYSTEM | OMP | Substantially Equivalent | Talley Medical | accessdata.fda.gov |
Compare with other makers
- All makers of Negative Pressure Wound Therapy Powered Suction Pump
- All makers of Mattress, Air Flotation, Alternating Pressure
Updated February 19, 2016. 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.