Data / Medical devices / Spain / Implant Protesis Dental 2004, S.L.
Implant Protesis Dental 2004, S.L.: FDA-registered device maker in Premia de Dalt Barcelona, Spain, 7 510(k) clearances
Implant Protesis Dental 2004, S.L. is registered with the FDA (registration 3016954909) in Premia de Dalt Barcelona, Spain. It lists 5 device types. The FDA files 7 510(k) clearances under its listings, the newest dated January 22, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3016954909
- Address
- Carrer Rosa dels Vents, 9-15, Premia de Dalt Barcelona, Spain, 08338
- Owner or operator
- IMPLANT PROTESIS DENTAL 2004, S.L. (10086489)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- November 14, 2022
- Registered through
- 2026
- Brand names listed
- Analog C/X, Analog GM small, Analog Low profile diam. 4.8, Analog NP, Analog NT, Analog Narrow NP, Analog PSD, Analog RB and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Abutment, Implant, Dental, Endosseous | NHA | 2 | Manufacturer | accessdata.fda.gov |
| Accessories, Implant, Dental, Endosseous | NDP | 1 | Manufacturer | accessdata.fda.gov |
| Dental Abutment Design Software For Dental Laboratory | PNP | 2 | Manufacturer | accessdata.fda.gov |
| Handle, Instrument, Dental | EJB | 1 | Manufacturer | accessdata.fda.gov |
| System, Image Processing, Radiological | LLZ | 2 | Exporter to the US | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| January 22, 2026 | K253253 | IPDmilled Blanks | NHA | Substantially Equivalent | Implant Protesis Dental 2004, S.L. | accessdata.fda.gov |
| August 20, 2025 | K251471 | IPD Dental Implant Abutments | NHA | Substantially Equivalent | Implant Protesis Dental 2004, S.L. | accessdata.fda.gov |
| December 19, 2024 | K242819 | IPD Dental Implant Abutments | NHA | Substantially Equivalent | Implant Protesis Dental 2004, S.L. | accessdata.fda.gov |
| June 7, 2024 | K240570 | IPD Dental Implant Abutments | NHA | Substantially Equivalent | Implant Protesis Dental 2004, S.L. | accessdata.fda.gov |
| October 10, 2023 | K231413 | IPD Dental Implant Abutments | NHA | Substantially Equivalent | Implant Protesis Dental 2004, S.L. | accessdata.fda.gov |
| October 21, 2022 | K222215 | IPD Dental Implant Abutments | NHA | Substantially Equivalent | Implant Protesis Dental 2004, S.L. | accessdata.fda.gov |
| December 20, 2018 | K173041 | 3DIEMME RealGUIDE | LLZ | Substantially Equivalent | 3Diemme , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Dental Abutment Design Software For Dental Laboratory
- All makers of Abutment, Implant, Dental, Endosseous
- All makers of System, Image Processing, Radiological
- All makers of Handle, Instrument, Dental
- All makers of Accessories, Implant, Dental, Endosseous
Updated January 22, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.