FDA Device Intelligence
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Legging, Compression, Non-Inflatable

FDA product code LLK · Class 2 · General Hospital

3
Registered devices
25
Adverse events
1
Recalls
4
510(k) clearances

Devices with this code

CopperUnder sock Large — SUN SCIENTIFIC, INC.CopperUnder sock Small/Medium — SUN SCIENTIFIC, INC.CopperUnder sock Extra Large — SUN SCIENTIFIC, INC.

Recent recalls

DateFirmReason
2014-10-08Customed, IncCustomed products are being recalled because of compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.