COCOMO GLOBAL CO., LTD

FDA Device Registration & Listing · Bao Vinh Ward Dong Nai, VN · Registration 3018101395

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
3018101395
FEI Number
3018101395
Entity Name
COCOMO GLOBAL CO., LTD
City/State/Country
Bao Vinh Ward Dong Nai, VN
Establishment Address
No.50/3, Group 26, Bao Vinh B Area, Bao Vinh Ward Dong Nai 76459, VN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Cocomo Global Co., Ltd (Owner Number: 10080898)
Owner / Operator Contact Address
No. 50/3, Group 26, Bao Vinh B Area, Bao Vinh Ward, Long Khanh, VN-39 76459, VN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Bubble Overlay with air pump Disposable Blood Pressure Cuffs

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DXQ Blood Pressure Cuff Cardiovascular Class 2 870.1120 2022-02-21
IKY Mattress, Flotation Therapy, Non-Powered General Hospital Class 1 880.5150 2025-12-10
DXQ Blood Pressure Cuff Cardiovascular Class 2 870.1120 2021-04-15

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Cocomo Global 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
K831001 Frontier Products UNICUFF-BLOOD PRESSURE CUFF 1983-07-28
K253089 Shenzhen Best Electronics Co., Ltd. NIBP Cuff (BCS-112, BCS-212, BCS-312, BCS-412, BCS-512, BCS-612, BCS-712, BCS-122, BCS-222, BCS-322, BCS-422, BCS-522, BCS-622, BCS-722, BCD-112, BCD-212, BCD-312, BCD-412, BCD-512, BCD-612, BCD-712, BCD-122, BCD-222, BCD-322, BCD-422, BCD-522, BCD-622, BCD-722) 2026-02-13
K972301 Rudolf Riester GmbH & Co. KG BIG BEN SQUARE, BIG BEN ROUND 1997-09-17

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3018101395. Last updated year: 2026. Please use registration number 3018101395 when referencing this establishment in official correspondence.
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