FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)

What changed & why it matters

Med Spa Radar recorded an FDA import refusal at the federal level, dated July 24, 2026, in the Aesthetic Injectables category.

An import refusal marks a shipment the FDA stopped at the U.S. border as violative — the gray-market corridor a med spa must never source injectables from. Foreign, unapproved, or misbranded product refused at import is exactly what surfaces when a practice buys outside verified US-licensed 503A/503B or FDA-registered channels.

Type

FDA Import Refusal

Jurisdiction

Federal

Category

Aesthetic Injectables

Recorded

July 24, 2026

What this means for your specific practice — the exact step to take, the deadline to calendar, or the supplier detail to check — is in the member "what to do" below. This page is the free record of what changed and why it matters.

What to do

The FDA record

Firm

Forest Hills Lab Korea Co Ltd

Origin

Gyeonggi-do, South Korea

Product

Implant, Dermal, Collagen For Aesthetic Use

FDA classification

General and Plastic Surgery Medical Devices

Refused

Jul 24, 2026

FDA district

Division of Southeast Imports

Firm FEI

3027803824

FDA shipment ID

AEK-0699449-4/10002/1A

Why FDA refused it

• Misbranding502(o), 801(a)(3); MISBRANDING

  It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

• Adulteration501(f)(1)(B), 801(a)(3); ADULTERATION

  The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

• Misbranding502(o), 801(a)(3); MISBRANDING

  The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

FDA charge codes on this record: 118 (Misbranding) · 237 (Adulteration) · 3280 (Misbranding). Definitions via the FDA Refusal Charges Reference.