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VPro+ ASM-20023

by Propel Orthodontics LLC

VPro+ ASM-20023 is an orthodontic vibrator (FDA Class II; FDA product code OYH, Orthodontic Vibratory Accessory) made by Propel Orthodontics LLC, listed in FDA GUDID since 17 Mar 2020 (UDI-DI 00852673007189), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00852673007189 UDI-DI Date17 Mar 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
VPro+
Generic name
Orthodontic vibrator
Model / reference
ASM-20023
Primary DI / UDI-DI
00852673007189
FDA product code
OYH
GMDN term
Orthodontic vibrator
Device class
Class II
Regulation number
872.5470
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code OYH (Orthodontic Vibratory Accessory).

Other devices from Propel Orthodontics LLC

See all devices from Propel Orthodontics LLC →

Properties

  • Contains latex
  • Prescription use
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (10, all answered No)