510(k) Report

FDA applicant

San Diego Swiss Machining, Inc.

San Diego, CA2 decisions1994–19960 recalls

FDA records 2 decisions for San Diego Swiss Machining, Inc. (San Diego, CA) from 1994 to 1996: 2 510(k) clearances. Most are in product codes ELC (Scaler, Ultrasonic) and EQH (Source, Carrier, Fiberoptic Light). 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 San Diego Swiss Machining, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for San Diego Swiss Machining, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — San Diego Swiss Machining, Inc. 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?

  • ELCScaler, Ultrasonic1decision
  • EQHSource, Carrier, Fiberoptic Light1decision

Who builds on its devices?

Later devices cite its devices 5 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K960889Sapphire Plus Scaler Mod. 300114/Plugger Mod. 300115/Cutting Mod. 300116/Spreader Mod. 300117 TipsSan Diego Swiss Machining, Inc. · 19965cite it

What has FDA decided for it lately?

  • K960889Sapphire Plus Scaler Mod. 300114/Plugger Mod. 300115/Cutting Mod. 300116/Spreader Mod. 300117 TipsSan Diego Swiss Machining, Inc. · 1996
  • K934911Saphire Plus Surgical MirrorSan Diego Swiss Machining, Inc. · 1994

All 2 as San Diego Swiss Machining, Inc. →