Acotec Scientific Co., Ltd.

FDA Device Registration & Listing · Beijing, CN · Registration 3015471899

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3015471899
FEI Number
3015471899
Entity Name
Acotec Scientific Co., Ltd.
City/State/Country
Beijing, CN
Establishment Address
4th, 5th Floor and North of 1st Floor, Building No.8, 16 Hongdabei Road, BDA, 100176 Beijing, China, 10th Longqing Street, BDA, 100176 Beijing, China, Beijing 100176, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Acotec Scientific Co.,Ltd. (Owner Number: 10090931)
Owner / Operator Contact Address
Courtyard No.10, Longqing Street Beijing Economic-Technological Development Area, Beijing, CN-BJ 100176, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Endovenous Radiofrequency Generator Cedar™ Endovenous Radiofrequency Catheters

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2025-11-18

Official Correspondent

Yan Li

US Agent Details

Anna Chan Business: Acotec Technologies, Inc. Email: anna.chan@acotec.com Phone: (612) 2221043

Related Public Records

Same Entity

Acotec Scientific Co.,Ltd.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K970809 Somnus Medical Technologies, Inc. BENDABLE TISSUE COAGULATING ELECTRODE WITH BENDING TOOL 1997-06-18
K222793 C.R. Bard, Inc. WavelinQ™ Generator 2022-10-17
K002257 Tecno Instruments (Pvt.) , Ltd. TECNO DISPOSABLE FINGERSWITCH PENCIL, MODEL 150-100 2000-10-19
K193591 Bowa-Electronics GmbH & Co. KG ARC 400 2020-04-02
K192128 Sutter Medizintechnik GmbH Sutter Arrowtip Monopolar Electrodes 2019-10-04

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0031-06 Rita Medical Systems 2
Rita Brand Habib 4X Electrosurgical Coagulator, Catalog Number: 4401US; Product is distributed by RITA Medical Systems, Inc., One Horizon Way. Manchester, GA 32826

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015471899. Last updated year: 2026. Please use registration number 3015471899 when referencing this establishment in official correspondence.
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