Hangzhou Kailong Medical Instruments Co., Ltd.

FDA Device Registration & Listing · Hangzhou Zhejiang, CN · Registration 3006789424

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
3006789424
FEI Number
3006789424
Entity Name
Hangzhou Kailong Medical Instruments Co., Ltd.
City/State/Country
Hangzhou Zhejiang, CN
Establishment Address
No. 558, Gaoerfu Road, Dongzhou, FuYang, Hangzhou Zhejiang 311401, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Hangzhou Kailong Medical Instruments Co., Ltd. (Owner Number: 10022985)
Owner / Operator Contact Address
No. 558, Gaoerfu Road, Dongzhou, FuYang, Hangzhou, CN-ZJ 311401, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

H1075X;H1075Y;H1075Z H2108X;H2108Y;H2108Z H1083X;H1083Y;H1083Z H8078 H2100X;H2100Y;H2100Z H2090X;H2090Y;H2090Z H41C H1077X;H1077Y;H1077Z H41 H2107X;H2107Y;H2107Z H7332 H6331X;H6331Y H1080X;H1080Y;H1080Z H2106X;H2106Y;H2106Z H1074X;H1074Y;H1074Z H1076X;H1076Y;H1076Z H2103X;H2103Y;H2103Z H5077M;H5077T H1088X H6043X;H6043Y H5177T-0.1/0.3-49 H6242X;H6242Y H8178-0.3/0.6-125 H6239X;H6239Y H1088Y H2092X;H2092Y;H2092Z H1086X;H1086Y;H1086Z H6884X;H6884Y H6240X;H6240Y H7332X

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ITY Assembly, Tube Housing, X-Ray, Diagnostic Radiology Class 1 892.1760 2007-10-29

Official Correspondent

Kai Ding

US Agent Details

Tom Howard Business: KAILONG USA Email: Thoward@kailong-Usa.com Phone: (608) 4380600

Related Public Records

Same Entity

Hangzhou Kailong Medical Instruments Co., Ltd.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006789424. Last updated year: 2026. Please use registration number 3006789424 when referencing this establishment in official correspondence.
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