Manufacturer registered with FDA
Vme Acquisition Corp.
Camarillo, CA, United States. Lists 1 dental device type with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.
- Device types listed
- 1
- Brands and models
- 0
- 510(k) clearances
- 11998–1998
- Markets registered in
- 11102 registrations outside the US
- Establishments
- 1United States
510(k) clearances per year, 1990–2026
Registered in 11 markets
Where regulators' registries name Vme Acquisition Corp. as the manufacturer or the registration holder of a device.
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Manufacturer | Vme Acquisition Corp. | 1 clearances | 1998–1998 | Below |
| Canada | Health Canada | Registration holder | KINAMED, INC. | 34 | 2002–2016 | Pure Global AI |
| Saudi Arabia | SFDA | Manufacturer | KINAMED, INC. | 26 | — | Pure Global AI |
| United Kingdom | MHRA | Manufacturer | Kinamed Inc. | 13 | — | Pure Global AI |
| Australia | TGA | Manufacturer | Kinamed Inc | 6 | 2006–2016 | Pure Global AI |
| Colombia | INVIMA | Registration holder | KINAMED INCORPORATED | 6 | — | Pure Global AI |
| Israel | AMAR | Manufacturer | Kinamed incorporated | 5 | — | Pure Global AI |
| Brazil | ANVISA | Manufacturer | KINAMED INCORPORATED | 4 | 2009–2014 | Pure Global AI |
| Peru | DIGEMID | Manufacturer | KINAMED, INC.KINAMED, INCORPORATED | 3 | 2018–2021 | Pure Global AI |
| Taiwan | TFDA | Manufacturer | KINAMED IncorporatedKINAMED INCORPORATED | 3 | 2015–2015 | Pure Global AI |
| China | NMPA | Registration holder | 科纳得公司Kinamed, Inc. | 2 | — | Pure Global AI |
Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026
Devices listed with FDA
What Vme Acquisition Corp. currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Intraosseous Fixation ScrewDZL · Class 2 | Maxillofacial plates & screws | Maker | — | 2008 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| KINAMED, INC.FDA reg. 2027148 | CAMARILLO, CA, United States | Manufacturer |
Other names on FDA records
Kinamed Inc.
Sources
FDA establishment registration & device listing (search FDA, owner/operator 2020352). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.