FDA applicant

Ross Implant Technologies Corp., Inc.

Washington, DC1 decision1986–19860 recalls

FDA records 1 decision for Ross Implant Technologies Corp., Inc. (Washington, DC) in 1986: 1 510(k) clearance. 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 Implant Technologies Corp., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ross Implant Technologies Corp., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ross Implant Technologies Corp., Inc. 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 Systems C/O Arent,Fox,Kintner,Plotkin,Kahn 2 Ross Research, Inc. 2 Ross Creek Medical, Inc. 1 Ross Medical Technology, Inc. 1 Ross Healthcare, Inc. 1

Ross Implant Technologies Corp., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Ross”