QINGDAO FUTURE MEDICAL TECHNOLOGY CO., LTD.

FDA Device Registration & Listing · Qingdao Shandong, CN · Registration 3014866140

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
3014866140
FEI Number
3014866140
Entity Name
QINGDAO FUTURE MEDICAL TECHNOLOGY CO., LTD.
City/State/Country
Qingdao Shandong, CN
Establishment Address
SouthB1 Building E,No.621 Jiushui Rd,Laoshan District, Qingdao Shandong 266000, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Qingdao Future Medical Technology Co., Ltd. (Owner Number: 10058479)
Owner / Operator Contact Address
South B1 Building E, No.621 Jiushui Rd, Laoshan District, Qingdao, CN-SD 266000, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Child Mask (H6) Adlut Mask (H6) Mouthpiece (H6) Intelligent Mesh Nebulizer (NEB001) Intelligent Mesh Nebulizer (NEB002) Nebulizer Accessory Set (H6HC) Mesh Nebulizer (H6) Nebulizer Cup (H6)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BYG Mask, Oxygen Anesthesiology Class 1 868.5580 2022-06-30
BYP Mouthpiece, Breathing Anesthesiology Class 1 868.5620 2022-06-30
CAF Nebulizer (Direct Patient Interface) Anesthesiology Class 2 868.5630 2018-10-04
BYG Mask, Oxygen Anesthesiology Class 1 868.5580 2025-12-18
BYP Mouthpiece, Breathing Anesthesiology Class 1 868.5620 2025-12-18
CAF Nebulizer (Direct Patient Interface) Anesthesiology Class 2 868.5630 2025-12-18
CCQ Nebulizer, Medicinal, Non-Ventilatory (Atomizer) Anesthesiology Class 1 868.5640 2021-05-20

Official Correspondent

Xinxin Wang

US Agent Details

Hui Hong Email: info@abmed.us Phone: (303) 8000162

Related Public Records

Same Entity

Qingdao Future Medical Technology 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
K163485 Adherium (Nz), Ltd. SmartTouch 2017-08-30
K781467 Travenol Laboratories, S.A. U-FLOAT VALVE 2D9023 1978-09-07

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014866140. Last updated year: 2026. Please use registration number 3014866140 when referencing this establishment in official correspondence.
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