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Data / Medical devices / Acid Phosphatase, Thymolphthale Inmonophosphate

Acid Phosphatase, Thymolphthale Inmonophosphate (CKE): 3 FDA-registered makers in 2 countries

3 establishments in 2 countries are registered with the FDA to make Acid Phosphatase, Thymolphthale Inmonophosphate (product code CKE, Class 2, 21 CFR 862.1020). 1 of them has a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 9 510(k) clearances under this code, the latest on March 17, 1992, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
CKE
Device class
2
Regulation
862.1020
Medical specialty
Clinical Chemistry

Makers by country

CountryMakers
United States2
Egypt1

Makers of Acid Phosphatase, Thymolphthale Inmonophosphate

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
Teco DiagnosticsAnaheim, CA, United StatesManufacturer1February 27, 1992000api.fda.gov
Elhoda Trade And SuppliesBadr industerial city Al Qahirah, EgyptManufacturer0000api.fda.gov
Siemens Healthcare Diagnostics Inc.Newark, DE, United StatesSpecification developer0000api.fda.gov

Updated March 17, 1992. 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.