Data / Medical devices / Germany / Page 3
FDA registered medical device manufacturers: 1,005, page 3
The full lists. FDA registered medical device manufacturers in Germany: 1,005 rows, $50.25, or the new rows each week for $19 a month. FDA registered medical device manufacturers and other establishments: 25,781 rows, $337.81, or the new rows each week for $19 a month. $10 of credit on sign-up, no card. Pay by card with no account. Prices exclude VAT. CSV and Excel files with the columns this page does not show (establishment name, FDA registration number, FEI number, street, city, state and 14 more), which open on your screen as soon as the payment clears and come by email. For agents and scripts: every list with its row count and price is at https://specstream.ai/data/lists.json.
Updated November 9, 2026. Source: openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files).
Manufacturers in Germany, 1,001 to 1,005 of 1,005, in the same order as page 1.
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 manufacturers 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.
Manufacturers in Germany, page 3
| Manufacturer | Location | FDA registration | Device types | 510(k) clearances | PMA approvals | Recall events | Source |
|---|---|---|---|---|---|---|---|
| macu4 GmbH | Konstanz Baden-Wurttemberg, Germany | 3042101018 | 3 | 0 | 0 | 0 | api.fda.gov |
| mebios GmbH | Dieburg Hesse, Germany | 3015131160 | 1 | 0 | 0 | 0 | api.fda.gov |
| medi-G GMBH | Messkirch Baden-Wurttemberg, Germany | 3001614464 | 8 | 0 | 0 | 0 | api.fda.gov |
| medi-plus Instrumente GmbH | TUTTLINGEN-NENDINGEN Baden-Wurttemberg, Germany | 8010935 | 24 | 0 | 0 | 0 | api.fda.gov |
| seleon gmbh | Heilbronn Baden-Wurttemberg, Germany | 3008606424 | 1 | 0 | 0 | 0 | api.fda.gov |
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. FDA registration lists an establishment with the FDA and is not an approval of it: a 510(k) clearance or a PMA approval is for one device. 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.
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