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Data / Medical devices / Tympanometer, Exempt

Tympanometer, Exempt (PTP): 4 FDA-registered makers in 4 countries

4 establishments in 4 countries are registered with the FDA to make Tympanometer, Exempt (product code PTP, Class 2, 21 CFR 874.1090). 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.

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Product code
PTP
Device class
2
Regulation
874.1090
Medical specialty
Ear, Nose, Throat

Makers by country

CountryMakers
Poland1
United States1
Russia1
Germany1

Makers of Tympanometer, Exempt

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
DGS Diagnostics Sp. z o.oKolbaskowo Zachodniopomorskie, PolandComplaint file establishment, Contract manufacturer0000api.fda.gov
Diagnostic Group LLCEden Prairie, MN, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
Neurosoft LtdIvanovo Ivanovskaya Oblast', RussiaManufacturer0000api.fda.gov
PathGermering Bavaria, GermanyManufacturer0000api.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.