510(k) Report

FDA applicant

Swiss Dental Center

San Luis Obispo, CA1 decision1997–19970 recalls

FDA records 1 decision for Swiss Dental Center (San Luis Obispo, CA) in 1997: 1 510(k) clearance. All are in product code DZE (Implant, Endosseous, Root-Form). Its devices cite 3 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Swiss Dental Center’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Swiss Dental Center since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Swiss Dental Center by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • DZEImplant, Endosseous, Root-Form1decision

Whose devices does it build on?

Its devices cite 3 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K954758Rootform Dental Implant SystemSwiss Dental Center · 1997

The one decision as Swiss Dental Center →

Other applicant names beginning “Swiss”

FDA records each applicant name separately; these may or may not be the same firm.

Swiss American Metal Craft Corp. 4Swiss American Products, Inc. 4Swiss Ray Medical Systems 3Swiss Orthopedic Solutions, Inc. 1Swiss Precision Mfg. Corp. 1Swiss Medical Care S.A. 1