CystoFlex™ F N

Catalogue number FP-10038, listed by Mauna KEA Technologies, France, under Confocal Optical Imaging. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
16510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (1), Shandong (1), Jiangsu (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code OWN
Manufacturer City Province Registered as Device types
Qingdao O-MEC Medical Technology Co., Ltd. Qingdao Shandong Contract manufacturer 6
Guangdong Optomedic Technologies, Inc. Foshan Guangdong Manufacturer 7
Wuxi Hisky Medical Technologies Co., Ltd. Wuxi Jiangsu Manufacturer 4

Record

Regulatory record for CystoFlex™ F N
Listed by Mauna KEA Technologies, France
FDA product code OWN
Device type Confocal Optical Imaging
Device class Class 2
Regulation 21 CFR 876.1500
Establishment Manufacturer
510(k) K193416
Record published 2020-05-15
Record revised 2021-07-26 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation High-level Disinfectant
Prescription Prescription only
Label carries expiry date, manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for CystoFlex™ F N
Catalogue number Size Status
FP-10038 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
VS3-IR Visionsense, Ltd. 22
Confocal Microprobe Imaging System Wuxi Hisky Medical Technologies Co., Ltd. 16
Confocal Optical Imaging Karl Storz GmbH & Co. KG 13
Hopkins Karl Storz GmbH & Co. KG 4
AIM (Advanced Imaging Modality) Stryker GmbH 4
VS3-NE Visionsense, Ltd. 3
Open Field Fluorescence Imaging Head Guangdong Optomedic Technologies, Inc. 3
Cellvizio® 100 series (488nm) Mauna KEA Technologies 3
Photonvue Fluoptics SAS 2
VS3 Iridium Visionsense, Ltd. 2
SafeLight Stryker GmbH 2
1588 AIM Stryker GmbH 2

Showing 12 of 74. All products under Confocal Optical Imaging

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K220477 2022-04-11
K212322 2021-08-18
K193416 2020-02-28
K191144 2020-01-24
K183640 2019-02-22
K172844 2017-12-15
K171345 2017-08-04
K160416 2016-05-20
K150831 2015-12-22
K151593 2015-10-23
K141358 2014-09-25
K133466 2014-07-25
K123676 2013-04-18
K122042 2012-09-04
K120208 2012-04-20
K111047 2011-08-08

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer