Home / Import refusals / AEK-0493626-5/10002/1C

FDA Import Refusal AEK-0493626-5/10002/1C — Medytox Inc.

Medytox Inc. — FEI 3014451374

The FDA refused shipment AEK-0493626-5/10002/1C from Medytox Inc. (South Korea) on August 13, 2026. The refused product falls under Devices — IMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE. Cited charge: 508 This firm has 5 or more other import refusals on record.

Refusal Details

Date
August 13, 2026
Country
South Korea
Product Category
Devices
Product Code
79LMH IMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
Charges
508

Other import refusals

  • 1FX-3667005-8/10002/1 (Fri Sep 25 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-9592353-6/10002/1A (Wed Sep 16 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 1FX-8156941-0/10002/1A (Wed Sep 09 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 1FX-6179109-1/10002/1 (Tue Aug 25 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-0766816-2/10002/1B (Tue Aug 18 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)

FDA data resources