2026 CBP ACE & FDA OASIS Enforcement Update: MoCRA Cosmetic FEI & QMSR Device 510(k) Affirmation of Compliance cross-checks are active at Los Angeles, Newark, Miami & Savannah ports.
FEILookup · DWPERadarFEI + OASIS + 483
OFFICIAL OPENFDA FEI RECORDFEI: 3044707950Reg Yr: 2026Vietnam (VN)

COMATRIX TECHNOLOGY VIETNAM COMPANY LIMITED

Official US Food and Drug Administration (FDA) Establishment Registration & Device/Facility Listing dossier for COMATRIX TECHNOLOGY VIETNAM COMPANY LIMITED (FEI 3044707950). Use this record to cross-check CBP ACE Affirmation of Compliance codes (`DEV` / `DFE` / `FEI`), verify the designated US Agent on file, and subscribe to automated Import Alert (DWPE) monitoring.

Registered Facility Address

No. 74, Lot CN17, Road No. 6, Dong An Industrial Park, Binh Hoa Ward, Ho Chi Minh City, Vietnam

Ho Chi Minh City, Vietnam (75208)

FDA FURLS Identifiers

FEI Number: 3044707950

Registration No: 3044707950 • Status Code: 1 (Active)

Designated U.S. Agent21 CFR 807.40

Leeyeo Kee

Regrek LLC

Dover, DE (USA)

302-6089028

regrek.cs@hotmail.com

Registered FDA Product Codes, Device Classes & Commercial Names

Cross-check your commercial invoice product descriptions against these active FDA product code filings to prevent NO_510K or UNAPPROVED_NEW_DRUG port holds.

Proprietary / Commercial Brand Names on File

STOCKING, MEDICAL SUPPORT
Product CodeFDA Classification NameDevice Class21 CFR Regulation510(k) Exempt?
MRIOrthosis, Truncal/Orthosis, LimbClass 121 CFR 890.3490 Requires 510(k) / Check
FSVP AUDIT WORKBOOKS & REAL-TIME OASIS DETENTION ALERTSFEI #3044707950 • Instant Delivery
5-Year Cleaned Excel Pack$39 One-Time

Download Normalized 5-Year Refusal, 483 & Recall Audit Workbook (.XLSX + CSV)

Includes all deduplicated overseas factory names, FEI/DUNS crosswalks, 5-year port refusal logs, plain-English statutory violation mappings, and FSVP supplier qualification templates ready for customs broker review.

  • Full 5-year OASIS refusal history for COMATRIX TECHNOLOGY VIETNAM COMPANY LIMITED (FEI 3044707950) + category peers
  • 21 CFR 1.505 Foreign Supplier Verification Program (FSVP) audit checklist tab
FEI #3044707950 Watchdog$15 / month

Instant Supplier Detention Webhook & Email Alert Monitor

Get an automated Slack/Webhook JSON payload and email alert within 15 minutes whenever FDA OASIS logs a new detention, Import Alert Red List addition, or Warning Letter for COMATRIX TECHNOLOGY VIETNAM COMPANY LIMITED (FEI 3044707950) before you wire your 70% balance payment.

Enter a corporate email address to receive FEI #3044707950 detention alerts.

Please enter a valid work email address (e.g., ops@company.com).

Optional HTTPS endpoint for automated JSON refusal payloads.

Please enter a valid https:// webhook URL or leave blank.

Other Verified FDA FEI Establishments in Vietnam

Frequently Asked Questions: FEI 3044707950 (COMATRIX TECHNOLOGY VIETNAM COMPANY LIMITED)

What is the FDA FEI Number for COMATRIX TECHNOLOGY VIETNAM COMPANY LIMITED?

According to public US FDA Establishment Registration records, COMATRIX TECHNOLOGY VIETNAM COMPANY LIMITED (Ho Chi Minh City, Vietnam) is assigned FDA Facility Establishment Identifier (FEI) 3044707950 (Registration No. 3044707950) with registration year 2026.

Who is the designated US Agent for FEI 3044707950 (COMATRIX TECHNOLOGY VIETNAM COMPANY LIMITED)?

The registered US Agent on file for FEI 3044707950 is Leeyeo Kee (Regrek LLC) located in Dover, DE. Importers should independently confirm active representation before filing CBP ACE entry.

Does an active FDA FEI registration guarantee that shipments from COMATRIX TECHNOLOGY VIETNAM COMPANY LIMITED will clear US Customs without detention?

No. An active FDA FEI number or establishment registration only confirms administrative listing in FDA FURLS. Shipments can still be detained at US ports under Detention Without Physical Examination (DWPE / Import Alerts) for labeling, 510(k), cGMP, or adulteration violations.