Skip to the page

Data / Medical devices / Multi-Analyte Controls, All Kinds (Assayed) / Germany

FDA-registered makers of Multi-Analyte Controls, All Kinds (Assayed) in Germany: 6 establishments

6 establishments in Germany are registered with the FDA to make Multi-Analyte Controls, All Kinds (Assayed) (product code JJY). 2 have a 510(k) clearance or PMA approval on file and 1 has a recall event. 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.

Device
Multi-Analyte Controls, All Kinds (Assayed)
Product code
JJY
Country
Germany

Makers of Multi-Analyte Controls, All Kinds (Assayed) in Germany

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Roche Diagnostics GMBHMANNHEIM Baden-Wurttemberg, GermanyExporter to the US, Manufacturer, Repackager or relabeler7September 1, 2010000api.fda.gov
Siemens Healthcare Diagnostics Products GmbHMARBURG Hesse, GermanyManufacturer2June 10, 2002000api.fda.gov
Chromsystems Instruments & Chemicals GMBHGräfelfing Bavaria, GermanyManufacturer0030api.fda.gov
DRG Instruments GMBHMARBURG Hesse, GermanyComplaint file establishment, Manufacturer0000api.fda.gov
Phadia GMBHFREIBURG Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Roche Diagnostics GMBHPENZBERG Bavaria, GermanyManufacturer, Specification developer0000api.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.