Data / Medical devices / India / Quickdent Devices Private Limited
Quickdent Devices Private Limited: FDA-registered device maker in Mumbai Maharashtra, India, 1 510(k) clearance
Quickdent Devices Private Limited is registered with the FDA (registration 3036779616) in Mumbai Maharashtra, India. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 19, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3036779616
- Address
- Unit No 128 Kuber Complex New Link Rd SN of village Oshiwar Link Rd Andheri Mumbai Suburban, Mumbai Maharashtra, India, 400053
- Owner or operator
- Quickdent Devices Private Limited (10092670)
- Roles
- Repackager or relabeler, Specification developer
- First device listed
- February 4, 2025
- Registered through
- 2026
- Brand names listed
- Quickdent Dental Implant System, Quickdent dental implant accessories
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Abutment, Implant, Dental, Endosseous | NHA | 2 | Specification developer | accessdata.fda.gov |
| Accessories, Implant, Dental, Endosseous | NDP | 1 | Specification developer | accessdata.fda.gov |
| Implant, Endosseous, Root-Form | DZE | 2 | Specification developer | accessdata.fda.gov |
| Non-Irrigation Endosseous Dental Implant Drill Bits | QRQ | 1 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| December 19, 2024 | K243094 | Quickdent Dental Implant System | DZE | Substantially Equivalent | Quickdent Devices Private , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Non-Irrigation Endosseous Dental Implant Drill Bits
- All makers of Accessories, Implant, Dental, Endosseous
- All makers of Abutment, Implant, Dental, Endosseous
- All makers of Implant, Endosseous, Root-Form
Updated December 19, 2024. 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.