510(k) Report

FDA applicant

Lorin Medical, Inc.

Boca Raton, FL1 decision1992–19920 recalls

FDA records 1 decision for Lorin Medical, Inc. (Boca Raton, FL) in 1992: 1 510(k) clearance. All are in product code DXQ (Blood Pressure Cuff). 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Lorin Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • DXQBlood Pressure Cuff1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K921997CUFF-MLorin Medical, Inc. · 19921cites it

What has FDA decided for it lately?

  • K921997CUFF-MLorin Medical, Inc. · 1992

The one decision as Lorin Medical, Inc. →

Other applicant names beginning “Lorin”

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

Lorin Technologies Corporation 1