Manufacturer registered with FDA
LX Precision Portugal, Unipessoal, Lda
Castelo de Paiva, Portugal. Lists 3 dental device types with FDA across 1 registered establishment.
- Device types listed
- 3
- Brands and models
- 16
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1Portugal
Devices listed with FDA
What LX Precision Portugal, Unipessoal, Lda currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Root-Form Endosseous ImplantDZE · Class 2 | Dental implants | Maker | SCREW VENT IMPLANT; TAPERED SCREW VENT IMPLANTSCREW-VENT DENTAL IMPLANT SYSTEMSPLINE DENTAL IMPLANT SYSTEM-TEMPORARY ABUTMENTSpline Implant SystemSPLINE TEMPORARY GINGIVAL CUFF AND IMPRESSION POST AND IMPLANT ANALOGSWISSPLUS IMPLANT SYSTEM, MODEL SPWB 8,10,12,14/OPH20/SMPR, SPB 8,10,12,14/OP3.5D/OPAR,OPB 8,10,12,14/OP2.3D/OP2.8DTapered Screw Vent Implant SystemZimmer Dental Inc.3.25 SPLINE TWIST IMPLANT, HA COATED | 2025 |
| Endosseous Dental Implant AbutmentNHA · Class 2 | Implant abutments | Maker | HEX-LOCK SHORT ABUTMENT, MODEL SA341, SA342, SA451, SA452, SA561, SA562ZIMMER CONTOUR PROVISIONAL COPINGZIMMER DENTAL HEX-LOCK PREPARED ABUTMENT (STRAIGHT & ANGLED)Zimmer Dental Inc.ZIMMER DENTAL ONE PIECE TAPERED ABUTMENT, MODELS TAC1, TACW1, TA5C1 | 2025 |
| Endosseous Dental Implant AccessoriesNDP · Class 1 | Implant instruments & surgical kits | Maker | Biomet 3i,LLC Implant AccessoriesZimmer Dental Implant Accessories | 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
| Establishment | Location | What it does |
|---|---|---|
| LX PRECISION PORTUGAL, UNIPESSOAL, LDAFDA reg. 3038136479 | Castelo de Paiva Aveiro, Portugal | Contract manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10092981). 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.