FDA applicant

Robert Bosch Corp.

St. James, NY21 decisions1979–19860 recalls

FDA records 21 decisions for Robert Bosch Corp. (St. James, NY) from 1979 to 1986: 21 510(k) clearances. Most are in product codes ESD (Hearing Aid, Air-Conduction, Prescription) and DRT (Monitor, Cardiac (Incl. Cardiotachometer &…). 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Robert Bosch Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Robert Bosch Corp.’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 “Robert”

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

Robert I. Chien & Assoc., Inc. 6 Robert R. Moore 5 Robert W. Bauer & Assoc., Inc. 3 Robert A James 2 Robert R. Stevens 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 Bosch Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Robert”