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Data / Medical devices / Accessories, Implant, Dental, Endosseous / India

FDA-registered makers of Accessories, Implant, Dental, Endosseous in India: 8 establishments

8 establishments in India are registered with the FDA to make Accessories, Implant, Dental, Endosseous (product code NDP). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Device
Accessories, Implant, Dental, Endosseous
Product code
NDP
Country
India

Makers of Accessories, Implant, Dental, Endosseous in India

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Dantech Digital Dental Solutions Private LimitedChennai Tamil Nadu, IndiaManufacturer0000api.fda.gov
Endonest Medical Systems LLPPALGHAR Maharashtra, IndiaManufacturer0000api.fda.gov
Kamal Encon Industries LimitedFaridabad Haryana, IndiaManufacturer0000api.fda.gov
Libral Traders Pvt. Ltd.New Delhi, IndiaManufacturer0000api.fda.gov
M/S Leixir Resources Pvt. LtdGURUGRAM Haryana, IndiaManufacturer0000api.fda.gov
Prevest Denpro LimitedJammu Jammu and Kashmir, IndiaManufacturer0000api.fda.gov
Quickdent Devices Private LimitedMumbai Maharashtra, IndiaSpecification developer0000api.fda.gov
Vedia Solutions, Division of Laxmi Dental LimitedPalghar Maharashtra, IndiaManufacturer, Repackager or relabeler0000api.fda.gov

Updated November 2, 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.