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Data / Medical devices / Non-Irrigation Endosseous Dental Implant Drill Bits

Non-Irrigation Endosseous Dental Implant Drill Bits (QRQ): 16 FDA-registered makers in 9 countries

16 establishments in 9 countries are registered with the FDA to make Non-Irrigation Endosseous Dental Implant Drill Bits (product code QRQ, Class 1, 21 CFR 872.3980). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 0 510(k) clearances under this code, and lists 0 recall events (0 Class I). 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.

Get every maker of this deviceMakers in the United StatesWatch this device
Product code
QRQ
Device class
1
Regulation
872.3980
Medical specialty
Dental

Makers by country

CountryMakers
United States4
Israel3
Pakistan2
Sweden2
South Korea1
Spain1
Switzerland1
Canada1
China1

Makers of Non-Irrigation Endosseous Dental Implant Drill Bits

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Bicon, LLCBoston, MA, United StatesSpecification developer0000api.fda.gov
Bioline Dental Implant Systems LtdMigdal Tefen Northern, IsraelManufacturer0000api.fda.gov
Comfort Surgical InstrumentsSialkot Punjab, PakistanManufacturer0000api.fda.gov
Confident InstrumentsSialkot Punjab, PakistanManufacturer0000api.fda.gov
Dmi Technology LLCLynbrook, NY, United StatesSpecification developer0000api.fda.gov
Dsi Dental Solutions LtdAshdod Southern, IsraelSpecification developer0000api.fda.gov
Micro Precision SwissSanta Ana, CA, United StatesContract manufacturer0000api.fda.gov
MK MeditechSeongnam-si Gyeonggi, South KoreaManufacturer0000api.fda.gov
Mozo-Grau SAValladolid, SpainExporter to the US, Manufacturer0000api.fda.gov
Nobel Biocare ABGOTEBORG Vastra Gotaland, SwedenSpecification developer0000api.fda.gov
Nobel Biocare AB, ProduktionKARLSKOGA Orebro, SwedenContract manufacturer0000api.fda.gov
Nobel Biocare Services AGKloten Zurich, SwitzerlandSpecification developer0000api.fda.gov
Paragon Implant MFG., LLCCalabasas, CA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
StomatotechPierrefonds Quebec, CanadaExporter to the US, Manufacturer, Specification developer0000api.fda.gov
Surcam Medical Devices And Developments LtdNahariya Northern, IsraelManufacturer0000api.fda.gov
Xiamen Xiang Ji Precision Machinery Technology Co., LtdXiamen Fujian, ChinaContract manufacturer, Manufacturer0000api.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.