What is FDA product code NQQ?

This device uses back-reflected light to create two-dimensional images versus back-reflected sound waves as are used in ultrasound imaging.

Radiology › DiagnosticSystem, Imaging, Optical Coherence Tomography (Oct)

Deeplive

Name: deepLive
Brand: deepLive

deepLive is intended to be used as a non-invasive imaging tool in the evaluation of external human tissue microstructure by providing three-dimensional, cross-sectional and en-face…

Registry build 21.09.26

deepLive is intended to be used as a non-invasive imaging tool in the evaluation of external human tissue microstructure by providing three-dimensional, cross-sectional and en-face real-time depth visualization for assessment by physicians to support in forming a clinical judgment.

2manufacturers in China registered for this device type

1catalogue number

2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (1), Guangdong (1).

Chinese manufacturers registered for FDA product code NQQ
Manufacturer	City	Province	Registered as	Device types
Micro-Tech (Nanjing) Co., Ltd.	Nan Jing	Jiangsu	Contract manufacturer	49
Shenzhen Vivolight Medical Device&Technology Co., Ltd.	Shenzhen	Guangdong	Manufacturer	4

Record

Regulatory record for deepLive
Listed by	Damae Medical, France
FDA product code	NQQ
Device type	System, Imaging, Optical Coherence Tomography (Oct)
Device class	Class 2
Regulation	21 CFR 892.1560
Establishment	Manufacturer
Record published	2025-09-24
Record revised	2026-05-07 (version 2)

Specifications

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

Catalogue Numbers

Catalogue numbers for deepLive
Catalogue number	Size	Status
OSP12		In distribution

Same Product Code

Other products under the same FDA product code
Product	Sold by	Catalogue numbers
Optis™	St. Jude Medical	13
Optis™	Lightlab Imaging, Inc.	11
Luminscan(TM) Disposable Imaging Kit	Micro-Tech (Nanjing) Co., Ltd.	9
Ilumien™	Lightlab Imaging, Inc.	6
Cornaris Intravascular Imaging System	Shenzhen Vivolight Medical Device&Technology Co., Ltd.	2
VivoSight	Michelson Diagnostics Ltd	2
AptiVue™	Lightlab Imaging, Inc.	2
Pantheris	Avinger, Inc.	2
NvisionVLE Imaging Console	Ninepoint Medical, Inc.	1
NvisionVLE Imaging Console Refurbished	Ninepoint Medical, Inc.	1
NvisionVLE Marking Probe 17mm	Ninepoint Medical, Inc.	1
NvisionVLE Low Profile Imaging Probe, 20mm Working Distance	Ninepoint Medical, Inc.	1

Showing 12 of 56. All products under System, Imaging, Optical Coherence Tomography (Oct)

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance	Decision date
K252851	2025-10-07
K240610	2024-07-09

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.