Manufacturer registered with FDA
Dntlworks Equipment Corp.
Centennial, CO, United States. Lists 5 dental device types with FDA across 1 registered establishment.
- Device types listed
- 5
- Brands and models
- 5
- 510(k) clearances
- 0as applicant
- Markets registered in
- 216 registrations outside the US
- Establishments
- 1United States
Registered in 2 markets
Where regulators' registries name Dntlworks Equipment 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 | Dntlworks Equipment Corp. | 5 device types | — | Below |
| Costa Rica | Ministerio de Salud | Manufacturer | DNTLWORKS EQUIPMENT CORP | 16 | — | 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 Dntlworks Equipment 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 |
|---|---|---|---|---|
| Dental Fiber Optic LightEAY · Class 1 | Dental operating lights | Maker | DNTLworks ProBrite | 2008 |
| Dental Operating LightEAZ · Class 1 | Dental operating lights | Maker | DNTLworks ProBrite | 2008 |
| Suction Operatory UnitEBR · Class 1 | Suction & evacuation units | Maker | NitrousVac portable vacuum unit | 2026 |
| Accessories Operative Dental UnitNRD · Class 1 | — | Maker | DNTLworks | 2008 |
| Dental Chair without Operative UnitNRU · Class 1 | Dental chairs & operative units | Maker | DNTLworks | 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 |
|---|---|---|
| DNTLWORKS EQUIPMENT CORP.FDA reg. 1721430 | Centennial, CO, United States | Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 9007493). 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.