Registered with FDA
CBE Pure Solutions Pty Ltd
Ferntree Gully, Australia. Lists 1 dental device type with FDA across 1 registered establishment.
- Device types listed
- 1
- Brands and models
- 0
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1Australia
Devices listed with FDA
What CBE Pure Solutions Pty 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 |
|---|---|---|---|---|
| Caries Detection DeviceLFC · Class 2 | Caries detection devices | Lister | — | 2025 |
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
CBE Pure Solutions Pty Ltd 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: Incisive Technologies Pty Ltd (1).
| Decided | 510(k) | Device | Applicant | Device type |
|---|---|---|---|---|
| 16 May 2023 | K222560 | BlueCheck Caries Detection & Monitoring | Incisive Technologies Pty Ltd | LFC Caries Detection Device |
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| CBE PURE SOLUTIONS PTY LTDFDA reg. 3032823828 | Ferntree Gully Victoria, Australia | Repacker / relabeler |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10094068). 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.