Manufacturer registered with FDA
STS Corporation
Duluth, GA, United States. Lists 4 dental device types with FDA across 1 registered establishment.
- Device types listed
- 4
- Brands and models
- 4
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1United States
Devices listed with FDA
What STS 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 |
|---|---|---|---|---|
| Irrigating (Dental) SyringeEIB · Class 1 | Dental hand instruments | Maker | Syringe, Irrigating, Dental - AMTC-K - EIB 1, Dental Hand Instrument | 2021 |
| Irrigating Endodontic Periodontic SyringeEIC · Class 1 | Dental hand instruments | Maker | Syringe, Periodontic, Endodontic, Irrigating - AMTC-K - EIC 1, Dental Hand Instrument | 2021 |
| Restorative and Impression Material SyringeEID · Class 1 | Dental hand instruments | Maker | Syringe, Restorative Impression Material - AMTC-K - EID 1, Dental Hand Instrument | 2021 |
| Cartridge SyringeEJI · Class 2 | Dental needles & syringes | Maker | Syringe, Cartridge, Dental - AMTC-K - EJI 2 | 2021 |
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 |
|---|---|---|
| STS CORPORATIONFDA reg. 3014150341 | Duluth, GA, United States | Complaint file establishment, Repacker / relabeler, Specification developer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10056102). 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.