FDA applicant

Robert Reid, Inc.

Chesterland, OH2 decisions2009–20100 recalls

FDA records 2 decisions for Robert Reid, Inc. (Chesterland, OH) from 2009 to 2010: 2 510(k) clearances. Most are in product codes HSB (Rod, Fixation, Intramedullary And Accessories) and MNI (Orthosis, Spinal Pedicle Fixation). Its devices cite 8 predicates, 0 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, orthopedic panel, where it files most

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

FDA decisions per year

1in 2010

2009high 1 (2009) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

FIG. 1 — Robert Reid, Inc. by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Robert Reid, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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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 R. Stevens 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 Reid, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Robert”