510(k) Report

FDA applicant

Dr. Joseph E. Grasso, D.D.S.

West Simsbury, CT3 decisions1996–19970 recalls

FDA records 3 decisions for Dr. Joseph E. Grasso, D.D.S. (West Simsbury, CT) from 1996 to 1997: 3 510(k) clearances. Most are in product codes DZE (Implant, Endosseous, Root-Form) and EGG (Attachment, Precision, All). 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 Dr. Joseph E. Grasso, D.D.S.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dr. Joseph E. Grasso, D.D.S. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dr. Joseph E. Grasso, D.D.S. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Dr. Joseph E. Grasso, D.D.S.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • DZEImplant, Endosseous, Root-Form2decisions
  • EGGAttachment, Precision, All1decision

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.

  • K950260Quick Coupling Device for Dental ProsthesesDr. Joseph E. Grasso, D.D.S. · 19971cites it

What has FDA decided for it lately?

  • K950261Device for Providing Quick Coupling for Dental ProsthesesDr. Joseph E. Grasso, D.D.S. · 1997
  • K950260Quick Coupling Device for Dental ProsthesesDr. Joseph E. Grasso, D.D.S. · 1997
  • K950259Coupling Device for Dental ProsthesisDr. Joseph E. Grasso, D.D.S. · 1996

All 3 as Dr. Joseph E. Grasso, D.D.S. →