VA170-SC

GUDID 04589551388936

NAKANISHI INC.

Ultrasonic dental scaling/debridement system
Primary Device ID04589551388936
NIH Device Record Key1f9e3dd5-efbf-4468-bd65-1d0351116249
Commercial Distribution StatusIn Commercial Distribution
Brand NameVA170-SC
Version Model NumberVA170-SC
Company DUNS690710546
Company NameNAKANISHI INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS104589551388936 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ELCScaler, ultrasonic

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2026-02-23
Device Publish Date2026-02-13

Devices Manufactured by NAKANISHI INC.

04589551388929 - VA170LUX-SC2026-02-23
04589551388936 - VA170-SC2026-02-23
04589551388936 - VA170-SC2026-02-23
04589551388981 - Potentiometer Set2026-02-23
04589551389452 - Varios2026-02-23
04589551383900 - Varios2026-02-23
04589551389476 - Perio Kit A2026-02-23
04589551389483 - VA1702026-02-23
04560264577763 - VA2-LUX-HP Ti2026-02-23

© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.