510(k) Report

FDA applicant

Telebrands Corp

Washington, DC2 decisions2003–20240 recalls

FDA records 2 decisions for Telebrands Corp (Washington, DC) from 2003 to 2024: 2 510(k) clearances. Most are in product codes IRP (Massager, Powered Inflatable Tube) and OAP (Laser, Comb, Hair). Its devices cite 1 predicate, 0 of them its own earlier devices. No recall is linked to its devices.

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

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

FIG. A — Illustration, physical medicine panel, where it files most

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

FDA decisions per year

1in 2024

2024: 1
2007high 1 (2024) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Telebrands Corp’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • IRPMassager, Powered Inflatable Tube1decision
  • OAPLaser, Comb, Hair1decision

Whose devices does it build on?

Its devices cite 1 predicate; 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.

  • K032505Air Press MassagerTelebrands Corp · 20031cites it

What has FDA decided for it lately?

  • K240689Robin's EggTelebrands Corporation · 2024
  • K032505Air Press MassagerTelebrands Corp · 2003

The one decision as Telebrands Corp →The one decision as Telebrands Corporation →