FDA applicant

Suredrop, Inc.

Tiger, GA2 decisions1988–19890 recalls

FDA records 2 decisions for Suredrop, Inc. (Tiger, GA) from 1988 to 1989: 2 510(k) clearances. All are in product code JYJ (Gauge, Measuring). 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, ear, nose and throat panel, where it files most

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

FDA decisions per year

No FDA decision for Suredrop, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Suredrop, 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

Suredrop, Inc.

Which product codes does it file in?

What has FDA decided for it lately?