FDA applicant

Ross Systems C/O Arent,Fox,Kintner,Plotkin,Kahn

Washington, DC2 decisions1987–19890 recalls

FDA records 2 decisions for Ross Systems C/O Arent,Fox,Kintner,Plotkin,Kahn (Washington, DC) from 1987 to 1989: 2 510(k) clearances. All are in product code DZE (Implant, Endosseous, Root-Form). 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 Ross Systems C/O Arent,Fox,Kintner,Plotkin,Kahn’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ross Systems C/O Arent,Fox,Kintner,Plotkin,Kahn since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ross Systems C/O Arent,Fox,Kintner,Plotkin,Kahn by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Ross”

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

Ross Products 4 Ross Product Div. Abbott Laboratories 4 Ross Research, Inc. 2 Ross Creek Medical, Inc. 1 Ross Implant Technologies Corp., Inc. 1 Ross Medical Technology, Inc. 1 Ross Healthcare, Inc. 1

Ross Systems C/O Arent,Fox,Kintner,Plotkin,Kahn

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Ross”