FDA applicant

Robert R. Stevens

Miami Lakes, FL2 decisions1996–19970 recalls

FDA records 2 decisions for Robert R. Stevens (Miami Lakes, FL) from 1996 to 1997: 2 510(k) clearances. Most are in product codes KOC (Accessories, Blood Circuit, Hemodialysis) and DXC (Clamp, Vascular). Its devices cite 1 predicate, 1 of them its own earlier devices. 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, gastroenterology and urology panel, where it files most

How often FDA has decided Robert R. Stevens’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Robert R. Stevens since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Robert”

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

Robert Bosch Corp. 21 Robert I. Chien & Assoc., Inc. 6 Robert R. Moore 5 Robert W. Bauer & Assoc., Inc. 3 Robert A James 2 Robert Reid, Inc. 2 Robert B. Scott Ocularists of Florida, Inc. 2 Robert J. Sislian, Inc. 1 Robert C. Cameron 1 Robert Shaw Controls Co. 1 Robert C. Leif, Ph.D. 1 Robert Bosch Healthcare Systems, Inc. 1

Robert R. Stevens

Which product codes does it file in?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Robert”