OFFICIAL OPENFDA FEI RECORDFEI: 3012041047Reg Yr: 2027China (CN)

JIANGXI DENTALBRIGHT TECHNOLOGY CO., LTD

Official US Food and Drug Administration (FDA) Establishment Registration & Device/Facility Listing dossier for JIANGXI DENTALBRIGHT TECHNOLOGY CO., LTD (FEI 3012041047). 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

Makou industrial park, Yongxiu County

Jiujiang City Jiangxi, China (330300)

FDA FURLS Identifiers

FEI Number: 3012041047

Registration No: 3012041047 • 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

Teeth Wipes, Brush Ups, Finger Brush, Oral Brush Ups, Bamboo toothbrush, Plastic toothbrush,toothbrush, bamboo toothbrush, Travel Kit Toothbrush & Toothpaste tablets/(refill)

Product Code	FDA Classification Name	Device Class	21 CFR Regulation	510(k) Exempt?
EFW	Toothbrush, Manual	Class 1	21 CFR 872.6855	Requires 510(k) / Check

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21 CFR 1.505 Foreign Supplier Verification Program (FSVP) audit checklist tab

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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 JIANGXI DENTALBRIGHT TECHNOLOGY CO., LTD (FEI 3012041047) before you wire your 70% balance payment.

URGENT U.S. FDA & CUSTOMS COMPLIANCE COUNSEL DISPATCH

Respond-By Deadline Priority Triage

Shipment Detained by FDA or Placed on Import Alert? Request Free 24h Detention Evaluation from Licensed US FDA Compliance Counsel

When FDA issues a Notice of FDA Action (Detention), importers typically have only 10 to 20 business days to file a Form FDA 766 relabeling application, submit an accredited private laboratory packet (PLAP), or petition for Import Alert Red List removal before CBP orders refusal and liquidated damages.

Your Full Name & Role (Required)

Include your name and title (e.g., “Sarah Chen, VP Supply Chain”).

Please provide your full name (at least 2 characters).

Work Email for 24h Legal Memo (Required)

Used strictly to deliver your conflict-free 24h FDA detention evaluation.

Please enter a valid corporate email address.

Importer Website or Amazon/Shopify Store URL (Required)

Include https:// so counsel can pre-screen product Intended Use claims.

Please enter a valid URL starting with https:// or http://.

CBP Entry Number or Supplier FEI # (Required)

Format: 10-digit FEI (e.g., 3012041047) or 11-char CBP Entry # (e.g., W94-8829104-3).

Enter a 5–24 character alphanumeric FEI number or CBP Entry number.

US Port of Detention

Select the FDA District / Port holding the cargo.

Primary Cited FDA Charge Code

Charge listed on your Notice of FDA Action.

Commercial Cargo Value at Risk

Determines Form 766 vs. PLAP economic viability.

Notice of FDA Action Summary & Respond-By Date (Optional)

Describe whether cargo is currently on hold in ITACS, whether private lab sampling has started, or if you need an Import Alert removal petition.

🔒 Confidential submission • Zero upfront cost for 24h detention evaluation • Matched with licensed US FDA / Customs attorneys.

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Frequently Asked Questions: FEI 3012041047 (JIANGXI DENTALBRIGHT TECHNOLOGY CO., LTD)

What is the FDA FEI Number for JIANGXI DENTALBRIGHT TECHNOLOGY CO., LTD?

According to public US FDA Establishment Registration records, JIANGXI DENTALBRIGHT TECHNOLOGY CO., LTD (Jiujiang City Jiangxi, China) is assigned FDA Facility Establishment Identifier (FEI) 3012041047 (Registration No. 3012041047) with registration year 2027.

Who is the designated US Agent for FEI 3012041047 (JIANGXI DENTALBRIGHT TECHNOLOGY CO., LTD)?

The registered US Agent on file for FEI 3012041047 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 JIANGXI DENTALBRIGHT TECHNOLOGY CO., LTD 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.