Pde-Neo

Catalogue number C10935-40, listed by Hamamatsu Photonics K.K., Japan, 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
1510(k) clearance

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 pde-neo
Listed by Hamamatsu Photonics K.K., Japan
FDA product code OWN
Device type Confocal Optical Imaging
Device class Class 2
Regulation 21 CFR 876.1500
510(k) K133719
Record published 2016-09-23
Record revised 2018-07-06 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries expiry date, manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for pde-neo
Catalogue number Size Status
C10935-40 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
K110480 2012-01-13

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