Manufacturer registered with FDA
Florida Probe Corp.
Gainesville, FL, United States. Lists 1 dental device type with FDA across 1 registered establishment, and holds 2 510(k) clearances as applicant.
- Device types listed
- 1
- Brands and models
- 1
- 510(k) clearances
- 21988–1989
- Markets registered in
- 45 registrations outside the US
- Establishments
- 1United States
510(k) clearances per year, 1980–2026
Registered in 4 markets
Where regulators' registries name Florida Probe 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 | Florida Probe Corp. | 2 clearances | 1988–1989 | Below |
| Australia | TGA | Manufacturer | Florida Probe Corporation | 2 | 2006–2022 | Pure Global AI |
| South Korea | MFDS | Manufacturer | Florida Probe Corporation | 2 | 2004–2016 | Pure Global AI |
| China | NMPA | Registration holder | 佛罗里达探针公司Florida Probe Corporation | 1 | — | 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 Florida Probe 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 |
|---|---|---|---|---|
| Periodontic ProbeEIX · Class 1 | Dental hand instruments | Maker | THE FLORIDA PROBE | 1992 |
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 |
|---|---|---|
| FLORIDA PROBE CORP.FDA reg. 1039382 | GAINESVILLE, FL, United States | Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 1039382). 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.