510(k) Report

FDA applicant

Sun Ind., Inc.

Jonesboro, AR2 decisions1980–19941 recall

FDA records 2 decisions for Sun Ind., Inc. (Jonesboro, AR) from 1980 to 1994: 2 510(k) clearances. All are in product code LEJ (Booth, Sun Tan). 1 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, general and plastic surgery panel, where it files most

How often FDA has decided Sun Ind., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sun Ind., Inc. since 2007.

Recalls per year

1in 2014

2014: 1
2007high 1 (2014) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Sun Ind., Inc.’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?

  • LEJBooth, Sun Tan2decisions

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.

  • K800744Suntana Sunbed #SB-1 & Sunbrella #SU-1Sun Ind., Inc. · 19801cites it

What has FDA decided for it lately?

  • K932483SundashSun Ind., Inc. · 19941 recall
  • K800744Suntana Sunbed #SB-1 & Sunbrella #SU-1Sun Ind., Inc. · 1980

All 2 as Sun Ind., Inc. →

What has been recalled?

1 recall linked to its devices; the latest:

  • K932483SUN DASH RADIUS 252 PN 8000809705. The device is intended to be used for the tanning of…Jul 25, 2014Class II