FDA applicant

Richard Ting

Philadelphia, PA1 decision1997–19970 recalls

FDA records 1 decision for Richard Ting (Philadelphia, PA) in 1997: 1 510(k) clearance. All are in product code ELW (Material, Impression). 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 Richard Ting’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Richard Ting since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Richard Ting by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Richard Ting’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

Other applicant names beginning “Richard”

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

Richard Wolf Medical Instruments Corp. 155 Richard'S Medical Equip., Inc. 48 Richard-Allan Medical Ind., Inc. 33 Richard-Allan Medical 8 Richard Hamer Assoc., Inc. 8 Richard F. Kronner, M.D. 3 Richard James, Inc. 2 Richard Scott Elliott 1 Richard G. Deniro 1 Richard R. Anthony, M.D. 1 Richard D. Spradlin 1 Richard J. Turner Assoc. 1

Richard Ting

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Richard”