Manufacturer registered with FDA
Shenzhen Mold and Manufacturing Co Ltd
Shenzhen, China. Lists 10 dental device types with FDA across 1 registered establishment.
- Device types listed
- 10
- Brands and models
- 11
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1China
Devices listed with FDA
What Shenzhen Mold and Manufacturing Co Ltd 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 NeedleDZM · Class 1 | Dental needles & syringes | Maker | Syringe tip | 2012 |
| Resin Impression Tray MaterialEBH · Class 1 | Impression trays | Maker | Tray | 2012 |
| Heat Source for Bleaching TeethEEG · Class 1 | Teeth whitening lights | Lister | EvokeFutura 2400 | 2014 |
| Over the Counter Denture CleanserEFT · Class 1 | Denture cleansers & adhesives | Maker | Beaming White | 2016 |
| Manual ToothbrushEFW · Class 1 | Toothbrushes | Maker | Beaming White | 2013 |
| Polishing Agent StripEHM · Class 1 | Polishing & prophylaxis | Maker | Beaming White | 2015 |
| Preformed Impression TrayEHY · Class 1 | Impression trays | Maker | Tray | 2012 |
| All Types RetractorEIG · Class 1 | Dental hand instruments | Maker | Retractor | 2012 |
| Dental Plastic Filling InstrumentEIY · Class 1 | Dental hand instruments | Maker | Pen | 2013 |
| Dental Stain EraserMAU · Class 1 | — | Lister | Beaming White | 2019 |
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 |
|---|---|---|
| SHENZHEN MOYE TECHNOLOGY CO LTDFDA reg. 3009937681 | Shenzhen Guangdong, China | Contract manufacturer, Foreign exporter, Manufacturer, Repacker / relabeler |
Other names on FDA records
Shenzhen Moye Technology Co. Ltd.
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10042557). 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.