FDA applicant

Sage Products, Inc.

Crystal Lake, IL31 decisions1978–19980 recalls

FDA records 31 decisions for Sage Products, Inc. (Crystal Lake, IL) from 1978 to 1998: 31 510(k) clearances. Most are in product codes MMK (Container, Sharps) and FMH (Container, Specimen, Sterile). Its devices cite 2 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Sage Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Sage Products, Inc.’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 “Sage”

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

Sage Biopharma 6 Sage Pharmaceuticals, Inc. 2 Sage In-Vitro Fertilization, Inc. 2 Sage Laboratories, Inc. 1 Sage Electronics Products, Inc. 1

Sage Products, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Sage”