510(k) Report

FDA applicant

Grimm & Norton

Plainview, NY3 decisions1987–19900 recalls

FDA records 3 decisions for Grimm & Norton (Plainview, NY) from 1987 to 1990: 3 510(k) clearances. All are in product code JEY (Plate, Bone). 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 Grimm & Norton’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Grimm & Norton since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Grimm & Norton 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?

  • JEYPlate, Bone2decisions

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.

  • K901095BI-Phase Set, Oral, Maxillofacial SurgeryGrimm & Norton · 19901cites it

What has FDA decided for it lately?

  • K901095BI-Phase Set, Oral, Maxillofacial SurgeryGrimm & Norton · 1990
  • K901094Head Frame Kit, Oral Maxillofacial SurgeryGrimm & Norton · 1990
  • K872595Holding Rod, Surgical Forceps, Weinstein,12X2 3/4Grimm & Norton · 1987

All 3 as Grimm & Norton →

Other applicant names beginning “Grimm”

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

Grimm Scientific Industries, Inc. 3