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Data / Medical devices / Telescope, Laryngeal-Bronchial

Telescope, Laryngeal-Bronchial (ENZ): 4 FDA-registered makers in 2 countries

4 establishments in 2 countries are registered with the FDA to make Telescope, Laryngeal-Bronchial (product code ENZ, Class 2, 21 CFR 874.4680). 1 of them has a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 3 510(k) clearances under this code, the latest on September 15, 1995, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
ENZ
Device class
2
Regulation
874.4680
Medical specialty
Ear, Nose, Throat

Makers by country

CountryMakers
Germany3
Switzerland1

Makers of Telescope, Laryngeal-Bronchial

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
Karl Storz Se & Co KGTUTTLINGEN Baden-Wurttemberg, GermanySpecification developer1October 14, 1994000api.fda.gov
Karl Storz Se & Co. KGTUTTLINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Karl Storz Se & Co. KGNEUHAUSEN OBECK Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Storz Endoskop Produktions GMBHSchaffhausen, SwitzerlandContract manufacturer0000api.fda.gov

Updated September 15, 1995. 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.