Data / Medical devices / United Kingdom / Technovent Limited
Technovent Limited: FDA-registered device maker in Bridgend, United Kingdom, 1 510(k) clearance
Technovent Limited is registered with the FDA (registration 9617078) in Bridgend, United Kingdom. It lists 6 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 28, 2000. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9617078
- FEI number
- 3002876349
- Address
- UNit 5 York Park Bridgend Industrial Estate, Bridgend, United Kingdom, CF31 3TB
- Owner or operator
- TECHNOVENT LIMITED (9038802)
- Roles
- Manufacturer
- First device listed
- August 8, 2000
- Registered through
- 2026
- Brand names listed
- MagnaCap System, MagnaCap abutment, Magnamat, Spectromatch, Technovent Adhesive, Technovent Maxillofacial silicone system
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Attachment, Precision, All | EGG | 1 | Manufacturer | accessdata.fda.gov |
| Colorimeter, Photometer, Spectrophotometer For Clinical Use | JJQ | 1 | Manufacturer | accessdata.fda.gov |
| Implant, Endosseous, Root-Form | DZE | 2 | Manufacturer | accessdata.fda.gov |
| Material, External Aesthetic Restoration, Used With Adhesive | GBI | 1 | Manufacturer | accessdata.fda.gov |
| Prosthesis, Adhesive, External | GBJ | 1 | Manufacturer | accessdata.fda.gov |
| Tray, Surgical, Instrument | FSM | 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 |
|---|---|---|---|---|---|---|
| January 28, 2000 | K984297 | MAGNA ABUTMENT | DZE | Substantially Equivalent | Factor, Ii, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Colorimeter, Photometer, Spectrophotometer For Clinical Use
- All makers of Tray, Surgical, Instrument
- All makers of Material, External Aesthetic Restoration, Used With Adhesive
- All makers of Implant, Endosseous, Root-Form
- All makers of Attachment, Precision, All
- All makers of Prosthesis, Adhesive, External
Updated January 28, 2000. 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.