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Data / Medical devices / Splint, Endodontic Stabilizing

Splint, Endodontic Stabilizing (ELS): 4 FDA-registered makers in 4 countries

4 establishments in 4 countries are registered with the FDA to make Splint, Endodontic Stabilizing (product code ELS, Class 2, 21 CFR 872.3890). 1 of them has a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 6 510(k) clearances under this code, the latest on September 24, 1997, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
ELS
Device class
2
Regulation
872.3890
Medical specialty
Dental

Makers by country

CountryMakers
United States1
Germany1
Australia1
South Korea1

Makers of Splint, Endodontic Stabilizing

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
Practicon, Inc.Greenville, NC, United StatesManufacturer1February 25, 1994000api.fda.gov
Dentrade GMBH & Co.kgCologne North Rhine-Westphalia, GermanyManufacturer0000api.fda.gov
Inka Surgical InstrumentsJandakot Western Australia, AustraliaSpecification developer0000api.fda.gov
One Day Dental PartnerSuncheon-si Jeonnam, South KoreaExporter to the US, Manufacturer0000api.fda.gov

Updated September 24, 1997. 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.