Manufacturer registered with FDA
Baechler Feintech AG
Hoelstein, Switzerland. Lists 5 dental device types with FDA across 1 registered establishment.
- Device types listed
- 5
- Brands and models
- 5
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1Switzerland
Devices listed with FDA
What Baechler Feintech AG currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Powered Bone DrillDZI · Class 2 | Surgical drills & motors | Maker | Shaft f/Screwdriver 90° | 2025 |
| Manual Wire Driver and Bone DrillDZJ · Class 2 | Surgical drills & motors | Maker | Shaft f/Screwdriver 90° | 2025 |
| All Precision AttachmentEGG · Class 1 | — | Maker | Novaloc Matrix System | 2016 |
| Endosseous Dental Implant AccessoriesNDP · Class 1 | Implant instruments & surgical kits | Maker | Novaloc Matrix System | 2016 |
| Endosseous Dental Implant AbutmentNHA · Class 2 | Implant abutments | Maker | Medentika Abutment System | 2016 |
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 |
|---|---|---|
| BAECHLER FEINTECH AGFDA reg. 3010287737 | Hoelstein Basel-Landschaft, Switzerland | Contract manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10043105). 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.