FDA applicant

Super Sagless Corp.

Tupelo, MS2 decisions1990–19940 recalls

FDA records 2 decisions for Super Sagless Corp. (Tupelo, MS) from 1990 to 1994: 2 510(k) clearances. All are in product code FNL (Bed, Ac-Powered Adjustable Hospital). 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 Super Sagless Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Super Sagless Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Super”

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

Super Safe Plastic Products Co., Ltd. 6 Super Grow Lasers 2 Super Glide, Inc. 2 Super Optical, Inc. 1

Super Sagless Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Super”