FDA applicant

Ranir, LLC

Washington, DC9 decisions2006–20130 recalls

FDA records 9 decisions for Ranir, LLC (Washington, DC) from 2006 to 2013: 9 510(k) clearances. Most are in product codes OBR (Mouthguard, Over-The-Counter) and LRK (Device, Anti-Snoring). Its devices cite 21 predicates, 9 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Ranir Corporation”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

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

FDA decisions per year

1in 2013

2007high 2 (2009) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Ranir”

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

Ranir/Dcp Corp. 6

Ranir, LLC

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Ranir”