Registered with FDA
Wise Way (HK) Trading Limited
Wanchai, Hong Kong SAR China. Lists 2 dental device types with FDA across 1 registered establishment.
- Device types listed
- 2
- Brands and models
- 2
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1Hong Kong SAR China
Devices listed with FDA
What Wise Way (HK) Trading Limited currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Endosseous Dental Implant AbutmentNHA · Class 2 | Implant abutments | Lister | Dynamic Abutment Solutions | 2024 |
| Computer Assisted Design and Manufacturing (Cad/Cam) of Dental Restorations Optical Impression SystemNOF · Class 2 | Intraoral scanners | Lister | System, optical impression, computer assisted design and manufacturing (cad/cam) of dental restorations | 2017 |
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
Wise Way (HK) Trading Limited 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: Talladium Espana, SL (2).
| Decided | 510(k) | Device | Applicant | Device type |
|---|---|---|---|---|
| 17 Oct 2023 | K232151 | Dynamic TiBase | Talladium Espana, SL | NHA Endosseous Dental Implant Abutment |
| 4 May 2018 | K162021 | 3.0 Dynamic TiBase | Talladium Espana, SL | NHA Endosseous Dental Implant Abutment |
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| WISE WAY (HK) TRADING LIMITEDFDA reg. 3013960456 | Wanchai, Hong Kong SAR China | Foreign exporter |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10055803). 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.