Data / Medical devices / Italy / J Dental Care SRL
J Dental Care SRL: FDA-registered device maker in Modena, Italy, 5 510(k) clearances
J Dental Care SRL is registered with the FDA (registration 3013264549) in Modena, Italy. It lists 3 device types. The FDA files 5 510(k) clearances under its listings, the newest dated September 25, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013264549
- Address
- Via Dino Campana 2, Modena, Italy, 41123
- Owner or operator
- J DENTAL CARE SRL (10052880)
- Roles
- Manufacturer
- First device listed
- October 14, 2016
- Registered through
- 2026
- Brand names listed
- 15 Angulated Anatomic Abutment D 4.5 H 1.5 JDEvolution Plus, 15 Angulated Anatomic Abutment D 4.5 H 3 JDEvolution Plus, 17 Angulated Conical Abutment H 2.5 JDEvolution S, 26 mm Depth Probe JDNasal, 30 Angulated Conical Abutment H 2.5 JDEvolution S, 60mm Depth Probe JDZygoma, 60mm Straight Depth Probe JDZygoma, Abutment JDEvolution S 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 |
| Implant, Endosseous, Root-Form | DZE | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| September 25, 2025 | K251148 | JDEvolution Plus L and JDEvolution Plus LE | DZE | Substantially Equivalent | Jdentalcare Srl | accessdata.fda.gov |
| October 11, 2024 | K240143 | JDZygoma dental implants | DZE | Substantially Equivalent | Jdentalcare Srl | accessdata.fda.gov |
| August 16, 2024 | K233896 | JDentalCare Dental Implant System: JDEvolution; JDEvolution plus; JDIcon; JDIcon plus | DZE | Substantially Equivalent | Jdentalcare Srl | accessdata.fda.gov |
| June 26, 2020 | K182081 | JDentalCare Implant System JDIcon | DZE | Substantially Equivalent | Jdentalcare Srl | accessdata.fda.gov |
| November 6, 2015 | K143142 | JDENTALCARE Implant System | DZE | Substantially Equivalent | Jdentalcare Srl | accessdata.fda.gov |
Compare with other makers
- All makers of Implant, Endosseous, Root-Form
- All makers of Abutment, Implant, Dental, Endosseous
- All makers of Accessories, Implant, Dental, Endosseous
Updated September 25, 2025. 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.