Manufacturer registered with FDA

Schweizer Feinwerktechnik GmbH

Bad Boll, Germany. Lists 1 dental device type with FDA across 1 registered establishment.

FDA owner/operator10093456Contract manufacturer
Device types listed
1
Brands and models
65
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1Germany

Devices listed with FDA

What Schweizer Feinwerktechnik GmbH currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Endosseous Dental Implant AbutmentNHA · Class 2Implant abutmentsMaker
PREFIT10 3IC 3.4PREFIT10 3IC 4.1PREFIT10 3IC 5PREFIT10 3IC 6PREFIT10 BLX RBPREFIT10 BLX WBPREFIT10 KEP 3.5PREFIT10 KEP 4.1PREFIT10 KEP 5PREFIT10 KEX 5
55 more
PREFIT10 KEX 6.5PREFIT10 NBA 3.5PREFIT10 NBA 4.3/5PREFIT10 NBA 5.5PREFIT10 NBR 3.5PREFIT10 NBR 4.3PREFIT10 NBR 5PREFIT10 NBR 6PREFIT10 NGMPREFIT10 STB 2.9PREFIT10 STB 3.3PREFIT10 STB 4.1/4.8PREFIT10 STS 4.8PREFIT10 STS 6.5PREFIT10 TSV 3.5PREFIT10 TSV 4.5PREFIT10 TSV 5.7PREFIT14 3IC 4.1PREFIT14 3IC 5PREFIT14 3IC 6PREFIT14 BLX RBPREFIT14 BLX WBPREFIT14 KEP 3.5PREFIT14 KEP 4.1PREFIT14 KEP 5PREFIT14 KEX 5PREFIT14 KEX 6.5PREFIT14 NBA 3.5PREFIT14 NBA 4.3/5PREFIT14 NBA 5.5PREFIT14 NBR 3.5PREFIT14 NBR 4.3PREFIT14 NBR 5PREFIT14 NBR 6PREFIT14 NGMPREFIT14 STB 3.3PREFIT14 STB 4.1/4.8PREFIT14 STS 4.8PREFIT14 STS 6.5PREFIT14 TSV 3.5PREFIT14 TSV 4.5PREFIT14 TSV 5.7SCREW 3IC 3.4/4.1/5/6SCREW BLX RB/WBSCREW KEP 3.5/4.1/5SCREW NBA 3.5SCREW NBA 4.3/5SCREW NBR 3.5SCREW NBR 4.3/5/6SCREW NGMSCREW STB 2.9SCREW STB 3.3SCREW STB 4.1/4.8SCREW STS 4.8/6.5SCREW TSV 3.5/4.5/5.7
2025

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

EstablishmentLocationWhat it does
SCHWEIZER FEINWERKTECHNIK GMBHFDA reg. 3039397999Bad Boll Baden-Wurttemberg, GermanyContract manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10093456). 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.