510(k) Report

FDA applicant

The Merlin Corp.

Camarillo, CA2 decisions1994–19960 recalls

FDA records 2 decisions for The Merlin Corp. (Camarillo, CA) from 1994 to 1996: 2 510(k) clearances. Most are in product codes LRD (Applicator, Ent Drug) and BWF (Spirometer, Therapeutic (Incentive)). 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 The Merlin Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Merlin Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — The Merlin Corp. 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?

  • LRDApplicator, Ent Drug1decision
  • BWFSpirometer, Therapeutic (Incentive)1decision

What has FDA decided for it lately?

  • K953055Mistassist Breathing ExerciserThe Merlin Corp. · 1996
  • K942789MistassistThe Merlin Corp. · 1994

All 2 as The Merlin Corp. →

Other applicant names beginning “The”

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

Merlin Engineering Works, Inc. 8Merlin Medical Limited 2Merlin Group Dba Mcmerlin Dental Company 1