Skip to content

Prepair 200782

by Danville Materials, LLC

Prepair 200782 is a Class II device made by Danville Materials, LLC, listed in FDA GUDID since 22 Jun 2016 (UDI-DI 00816594021778), 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 Number00816594021778 UDI-DI Date22 Jun 2016ListedStatusListed 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  • Withdrawn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
Prepair
Generic name
Chairside dental abrasive air jet system control unit
Model / Ref / Catalog
200782
Primary DI / UDI-DI
00816594021778
FDA product code
KOJ
GMDN term
Chairside dental abrasive air jet system control unit
Device class
Class II
Regulation number
872.6080
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental abrasive air jet system control unit

Other devices from Danville Materials, LLC

See all devices from Danville Materials, LLC →

Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)