510(k) Report

FDA applicant

Glenwood, LLC

Tenafly, NJ2 decisions1997–19970 recalls

FDA records 2 decisions for Glenwood, LLC (Tenafly, NJ) in 1997: 2 510(k) clearances. All are in product code EFB (Handpiece, Air-Powered, Dental). Its devices cite 8 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 Glenwood, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Glenwood, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Glenwood, LLC 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?

  • EFBHandpiece, Air-Powered, Dental2decisions

Whose devices does it build on?

Its devices cite 8 predicates; 0 are its own earlier devices. The firms it cites most:

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.

  • K972376Impact Air 45 Handpiece for Periodontal UseGlenwood, LLC · 19971cites it
  • K972375Impact Air 45 Handpiece for Endodontic UseGlenwood, LLC · 19971cites it

What has FDA decided for it lately?

  • K972376Impact Air 45 Handpiece for Periodontal UseGlenwood, LLC · 1997
  • K972375Impact Air 45 Handpiece for Endodontic UseGlenwood, LLC · 1997

All 2 as Glenwood, LLC →