510(k) Report

FDA applicant

Accord Media

Los Gatos, CA1 decision2014–20144 recalls

FDA records 1 decision for Accord Media (Los Gatos, CA) in 2014: 1 510(k) clearance. All are in product code OLP (Over-The-Counter Powered Light Based Laser For…). 4 recalls are linked to its devices.

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

FIG. A — Illustration, general and plastic surgery panel, where it files most

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

FDA decisions per year

1in 2014

2014: 1
2014high 1 (2014) · low 0 (2015)2026

2026 so far, outlined.

Recalls per year

4in 2017

2017: 4
2014high 4 (2017) · low 0 (2014)2026

Class I Class II/III not classified

FIG. 1 — Accord Media by year, 2014–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

See the 510(k) Report

Which product codes does it file in?

  • OLPOver-The-Counter Powered Light Based Laser For Acne1decision

Who builds on its devices?

Later devices cite its devices 3 times; 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.

  • K132833Ultra Renew PlusAccord Media · 20143cite it

What has FDA decided for it lately?

  • K132833Ultra Renew PlusAccord Media · 20144 recalls

The one decision as Accord Media →

What has been recalled?

4 recalls linked to its devices; the latest:

  • K132833Ultra RenewDec 4, 2017Class II
  • K132833Truth RenewDec 4, 2017Class II
  • K132833Truth Renew PlusDec 4, 2017Class II
  • K132833Ultra Renew PlusDec 4, 2017Class II