CHONGQING BIO NEWVISION MEDICAL EQUIPMENT LTD.

FDA Device Registration & Listing · Chongqing, CN · Registration 3016589969

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
3016589969
FEI Number
3016589969
Entity Name
CHONGQING BIO NEWVISION MEDICAL EQUIPMENT LTD.
City/State/Country
Chongqing, CN
Establishment Address
2nd floor of building #5,27 Fengsheng Road,Jinfeng Town,High-Tech Industrial Development Zone, Chongqing 401329, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Chongqing Bio NewVision Medical Equipment Ltd. (Owner Number: 10062546)
Owner / Operator Contact Address
2nd floor of building #5,27 Fengsheng Road,Jinfeng Town,High-Tech Industrial Development Zone, Chongqing, CN-CQ 401329, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Fundus Camera RetiCam 3100 Fundus Camera Kestrel 3100m Fundus Camera,Model:Kestrel 300 Fundus Camera,Model:RetiCam 3100 Plus

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2020-02-11
PJZ Camera, Ophthalmic, General-Use Ophthalmic Class 2 886.1120 2023-10-18

Official Correspondent

Lishi Yin

US Agent Details

Wen Xu Email: infor@believe-med.com Phone: (443) 8968583

Related Public Records

Same Entity

Chongqing Bio NewVision Medical Equipment 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
K041546 Canon, Inc. DIGITAL FUNDUS CAMERA, MODEL CF-60DSI 2004-06-23

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0009-2018 Optovue, Inc. 2
iFusion, Device Listing Number D203271. Product Usage: The iCam is a non-contact, high resolution digital imaging device which is suitable for photographing, displaying and storing images of the retina and external areas of the eye to be evaluated under non-mydriatic conditions. The iCam takes digital images of the posterior and external structures of the eye without the use of a mydriatic agent and is intended for use as an aid to clinicians in the evaluation, diagnosis and documentation of ocular health. iCam provides images only and does not provide any diagnostic, pathological analysis or classification of ocular health or disease. AND iVue with Normative Database (K121739) - The iVue is a noncontact, high resolution optical coherence tomography system intended for in vivo imaging, axial cross-sectional, three-dimensional imaging and measurement of anterior and posterior. ocular structures, including retina, retinal nerve fiber layer, ganglion cell complex (GCC), optic disc, cornea, and anterior chamber of the eye. The iVue with Normative Database is a quantitative tool for comparison of retina, retinal nerve fiber layer, ganglion cell complex, and optic disc measurements to a database of known normal subjects.

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3010000450 CRYSTALVUE MEDICAL CORPORATION Taoyuan Dist.,, TW
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016589969. Last updated year: 2026. Please use registration number 3016589969 when referencing this establishment in official correspondence.
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