Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017259276

FEI Number

3017259276

Entity Name

VAPO HEALTHCARE CO., LTD.

City/State/Country

Suzhou Jiangsu, CN

Establishment Address

No. 99, Yudai West St., Kunshan National High-tech Industry Development Zone, Suzhou Jiangsu 215300, CN

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Vapo Healthcare Co., Ltd. (Owner Number: 10075694)

Owner / Operator Contact Address

No. 99, Yudai West St., Kunshan National High-tech Industry Development Zone, Suzhou, CN-JS 215300, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Nebulizer ear cleaner STETHOSCOPE Compressor Nasal Aspirator Electronic Thermometer Eye Masks,Eye Massager, Heated Eye Mask, Sleep Eye Masks,Steam Eye Masks, Bluetooth Eye Mask, Eye Heat Massager Eye Mask with white Noise breathing trainer

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
CCQ	Nebulizer, Medicinal, Non-Ventilatory (Atomizer)	Anesthesiology	Class 1	868.5640	2021-10-18
OGQ	Ear Irrigation Kit	General Hospital	Class 1	880.6960	2022-07-28
LDE	Stethoscope, Manual	Cardiovascular	Class 1	870.1875	2020-06-24
BTI	Compressor, Air, Portable	Anesthesiology	Class 2	868.6250	2020-07-13
KCP	Syringe, Ent	Ear, Nose, Throat	Class 1	874.5220	2021-10-19
SDV	Clinical Electronic Thermometer	General Hospital	Class 2	880.2910	2025-06-24
HOY	Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)	Ophthalmic	Class 1	886.4750	2025-01-24
ION	Exerciser, Non-Measuring	Physical Medicine	Class 1	890.5370	2021-03-14

Official Correspondent

Zhenning Jia

US Agent Details

Leeyeo Kee Business: Regrek LLC Email: regrek.cs@hotmail.com Phone: (302) 6089028

Related Public Records

Same Entity

Vapo Healthcare 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
K900686	Medical Industries America, Inc.	MAXI COMPRESSORS	1990-04-26

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017259276. Last updated year: 2026. Please use registration number 3017259276 when referencing this establishment in official correspondence.