Registered with FDA
Reset Technology Corporation
Irving, TX, United States. Lists 3 dental device types with FDA across 1 registered establishment.
- Device types listed
- 3
- Brands and models
- 3
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1United States
Devices listed with FDA
What Reset Technology Corporation currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Preformed Impression TrayEHY · Class 1 | Impression trays | Lister | Reset Impression Kit | 2024 |
| All Types RetractorEIG · Class 1 | Dental hand instruments | Lister | Reset Impression Kit | 2024 |
| Impression MaterialELW · Class 2 | Impression materials | Lister | ResetSmile Impression Kit | 2023 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Also lists devices cleared under other names
Reset Technology Corporation lists these devices with FDA today. The clearance names a different applicant, as happens after a rename, an acquisition or a private-label agreement.
Original applicants: Chemoment Materials Co.,ltd (1).
| Decided | 510(k) | Device | Applicant | Device type |
|---|---|---|---|---|
| 8 Aug 2022 | K221668 | Dental Impression Material | Chemoment Materials Co.,ltd | ELW Impression Material |
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| RESET TECHNOLOGY CORPORATIONFDA reg. 3030159375 | Irving, TX, United States | Repacker / relabeler |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10089702). 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.