510(k) Report

FDA applicant

Interdent, Inc.

Los Angeles, CA2 decisions1983–19980 recalls

FDA records 2 decisions for Interdent, Inc. (Los Angeles, CA) from 1983 to 1998: 2 510(k) clearances. Most are in product codes EIE (Dam, Rubber) and FLE (Sterilizer, Steam). 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 Interdent, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Interdent, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Interdent, 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?

  • EIEDam, Rubber1decision
  • FLESterilizer, Steam1decision

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K972775FastdamInterdent, Inc. · 19981cites it

What has FDA decided for it lately?

  • K972775FastdamInterdent, Inc. · 1998
  • K823457Non-Pressure Autoclave for SterilizationInterdent, Inc. · 1983

All 2 as Interdent, Inc. →