Z-SYSTEMS AG
1 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (1)
- Inspections (1)
- Warning letters (1)
Devices registered here (1)
- Implant, Endosseous, Root-FormProduct code DZE (opens in a new tab) · Class II · Dental · 21 CFR 872.3640
Recalls & enforcement
- Class IITerminated2013-05-16Devices labeled for an intended use not included in the existing 510(k) or PMA, in that, the user manual contains the Indication for Use of the soma v Platinum ABUS [a 510(k) product].
FDA inspections (1)
- OAI2024-04-25Official Action Indicated · Compliance: Devices · citations posted
Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.
FDA warning letters (1)
- Warning Letter2024-08-02Warning Letter (opens in a new tab) · Oensingen
Source: U.S. FDA Compliance Actions Dashboard (opens in a new tab) (device warning letters, 2016–present). Data as of 2026-10-06. Each link opens an FDA search for the letter; FDA can take several weeks to post a letter, so a very recent one may not appear yet.
Related
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Z-SYSTEMS AG (FEI 3006948427) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3006948427-z-systems-ag/
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