Manufacturer registered with FDA
Sanko Electronics Corporation
Midori, Japan. Lists 2 dental device types with FDA across 1 registered establishment.
- Device types listed
- 2
- Brands and models
- 26
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1Japan
Devices listed with FDA
What Sanko Electronics 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 |
|---|---|---|---|---|
| Handpiece and Cord Foot ControllerEBW · Class 1 | — | Maker | EL400JS120EL400S120FC-78NE136NE161NE188NE210NE278NL400B SET 5 TAKARA BELMONTNL400BSET5PCB 11 moreNL400BSET7NORACNL400S120NL400S120ENL400SBSET2BELNLX nano S120NLX nano S120ESurgic Pro NON-OPT(120V)Surgic Pro OPT(120V)Surgic Pro OPT(230V)Surgic Pro+ OPT(120V)TIM40S | 2022 |
| Ac-Powered Direct Drive HandpieceEKX · Class 1 | Dental handpieces | Maker | EMD120V1EMD120VSiProphy mobile complete setiProphy mobile MotorNE131 | 2022 |
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 |
|---|---|---|
| SANKO ELECTRONICS CORPORATIONFDA reg. 3025599428 | Midori Gunma, Japan | Contract manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10086958). 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.