Acteon

The C50 is an intraoral video camera equipped with LEDs to illuminate the inspection site. The C50 optics and its complementary metal oxide semiconductor (CMOS) sensor capture the natural…

Registry build 21.09.26

The C50 is an intraoral video camera equipped with LEDs to illuminate the inspection site. The C50 optics and its complementary metal oxide semiconductor (CMOS) sensor capture the natural fluorescence of the site under observation and convert the images into a video signal that is sent to the computer via a USB interface. The dental practitioner can use the images displayed on the computer screen as an aid in diagnosis. A USB Type-C (camera) to USB-A cable is provided to connect the C50 to a computer. The C50 provides the following functions: Aid in the detection of pit and fissure caries Information about patient dental hygiene Highlighting of dental plaque Highlighting of gingival inflammations (restricted to gingival inflammations which lead to bleeding upon probing) Showing the difference between “before” and “after” care (follow-up). In CARIO mode (blue mode), the camera assists the dental practitioner by highlighting potential carious areas in pits and fissures on the occlusal surface of the teeth. In DAYLIGHT mode (white mode), the camera enables visualization of anatomical details invisible to the naked eye or with a mirror (thanks to its magnification). DAYLIGHT+ mode (white mode) is a shortcut version of DAYLIGHT mode where the contrast has been pushed from 20 to 70. In PERIO mode (yellow mode), the camera helps the dental practitioner to visualize dental plaque, in addition to highlighting areas of gingival inflammation (restricted to gingival inflammation that leads to bleeding upon probing).

1manufacturer
13catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

Registered in Jiangsu.

Chinese manufacturers registered for FDA product code NBL
Manufacturer City Province Registered as Device types
Carl Zeiss Meditec (Suzhou) Co., Ltd. Suzhou Jiangsu Manufacturer 4

Record

Regulatory record for Acteon
Listed by Sopro, France
FDA product code NBL
Device type Light-Induced Fluorescence Caries Detector
Device class Class 2
Regulation 21 CFR 872.1745
Establishment Repacker / relabeller, Manufacturer
510(k) K223470
Record published 2019-03-12
Record revised 2020-12-04 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Supplied as a kit Yes
Label carries manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for Acteon
Catalogue number Size Status
KIT SOPROLIFE PAL with Mini Dock USB2 In distribution
CAMERA S900 NTSC SANS SUPPORT In distribution
SOPROLIFE NTSC STRAUMANN In distribution
SOPROLIFE NTSC In distribution
CAMERA S900 NTSC SOPROLIFE In distribution
C50 – INTRAORAL CAMERA In distribution
SOPROLIFE NTSC In distribution
CAMERA S900 NTSC SANS SUPPORT In distribution
SOPROLIFE N In distribution
SOPROLIFE PAL STRAUMANN In distribution
SOPROLIFE P In distribution
KIT SOPROLIFE NTSC with Mini Dock USB2 In distribution
CAMERA S900 NTSC SOPROLIFE In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Trios 3SHAPE Trios A/S 6
Trios 5 3SHAPE Trios A/S 3
Smartooth Smartooth Co., Ltd. 2
DIAGNOcam Vision Full HD Kavo Dental Gmbh 2
CS 1600 Carestream Health, Inc. 1
Primescan 2 Sirona Dental Systems Gmbh 1
Fluorescence Mode Carl Zeiss Suzhou Co., Ltd. 1
CamX Spectra Handpiece Dürr Dental SE 1
Primescan 2 Multiuse Sleeve Sirona Dental Systems Gmbh 1
Fluorescence Mode Carl Zeiss Meditec (Suzhou) Co., Ltd. 1
Ortek Therapeutics, Inc. Ortek Therapeutics, Inc. 1
Aiobio Aiobio Co., Ltd. 1

Showing 12 of 18. All products under Light-Induced Fluorescence Caries Detector

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K223470 2023-12-14
K121685 2013-03-12
K092583 2010-01-13

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