510(k) Report

FDA applicant

Nats Corp.

Sound Beach, NY5 decisions1999–20040 recalls

FDA records 5 decisions for Nats Corp. (Sound Beach, NY) from 1999 to 2004: 5 510(k) clearances. Most are in product codes DZE (Implant, Endosseous, Root-Form) and BSB (Warmer, Blood, Non-Electromagnetic Radiation). 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 Nats Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nats Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Nats Corp. 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
  • BSBWarmer, Blood, Non-Electromagnetic Radiation1decision
  • EBIResin, Denture, Relining, Repairing, Rebasing1decision
  • ILJBath, Hydro-Massage1decision
  • ITIWheelchair, Powered1decision

Who builds on its devices?

Later devices cite its devices 2 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.

  • K040143MonorailNats Corp. · 20041cites it
  • K020060AstofloNats Corp. · 20021cites it

What has FDA decided for it lately?

  • K040143MonorailNats Corp. · 2004
  • K033142Powered WheelchairNats Corp. · 2004
  • K020060AstofloNats Corp. · 2002
  • K011820Dentorium Convertible AcrylicNats Corp. · 2001
  • K991184Hydrotone-Thermal Capsule SystemNats Corp. · 1999

All 5 as Nats Corp. →