FDA applicant

Sage Pharmaceuticals, Inc.

Shreveport, LA2 decisions1995–19970 recalls

FDA records 2 decisions for Sage Pharmaceuticals, Inc. (Shreveport, LA) from 1995 to 1997: 2 510(k) clearances. All are in product code MGQ (Dressing, Wound And Burn, Hydrogel W/Drug…). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Sage Pharmaceuticals, 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 “Sage”

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

Sage Products, Inc. 31 Sage Biopharma 6 Sage In-Vitro Fertilization, Inc. 2 Sage Laboratories, Inc. 1 Sage Electronics Products, Inc. 1

Sage Pharmaceuticals, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Sage”