Manufacturer registered with FDA
Shenzhen Jiahong Dental Technology Co., Ltd
Shenzhen, China. Lists 7 dental device types with FDA across 1 registered establishment.
- Device types listed
- 7
- Brands and models
- 7
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1China
Devices listed with FDA
What Shenzhen Jiahong Dental Technology 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 |
|---|---|---|---|---|
| Resin Temporary Crown and BridgeEBG · Class 2 | Temporary crown & bridge materials | Maker | EBG | 2010 |
| Base Metal AlloyEJH · Class 2 | Dental alloys | Maker | EJH | 2009 |
| Gold-Based Noble Metal AlloyEJT · Class 2 | Dental alloys | Maker | EJT | 2010 |
| Denture Preformed (Partially Prefabricated Denture)EKO · Class 2 | Denture resins & teeth | Maker | EKO | 2010 |
| Porcelain TeethELL · Class 2 | Dental ceramics & zirconia | Maker | ELL | 2009 |
| Teeth Plastic DentureELM · Class 2 | Denture resins & teeth | Maker | ELM | 2009 |
| Endosseous Dental Implant AbutmentNHA · Class 2 | Implant abutments | Maker | NHA | 2010 |
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 Jiahong Dental Technology Co., LtdFDA reg. 3007740664 | Shenzhen Guangdong, China | Contract manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10029910). 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.