510(k) Report

FDA applicant

Lorin Technologies Corporation

Swansboro, NC1 decision2011–20110 recalls

FDA records 1 decision for Lorin Technologies Corporation (Swansboro, NC) in 2011: 1 510(k) clearance. All are in product code LFD (Saliva, Artificial). 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

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

FDA decisions per year

1in 2011

2011: 1
2011high 1 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — Lorin Technologies Corporation by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • LFDSaliva, Artificial1decision

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

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.

  • K110116Xeros Dry Mouth PumpLorin Technologies Corporation · 20111cites it

What has FDA decided for it lately?

  • K110116Xeros Dry Mouth PumpLorin Technologies Corporation · 2011

The one decision as Lorin Technologies Corporation →

Other applicant names beginning “Lorin”

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

Lorin Medical, Inc. 1