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Flexjet 8000-Opm

by Plasdent Corp.

Flexjet 8000-Opm is a Class I device made by Plasdent Corp., listed in FDA GUDID since 5 Jan 2022 (UDI-DI D8328000OPM1), 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 NumberD8328000OPM1 UDI-DI Date5 Jan 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Flexjet
Generic name
Dental suction system cannula, single-use
Model / Ref / Catalog
8000-OPM
Primary DI / UDI-DI
D8328000OPM1
FDA product code
DYN
GMDN term
Dental suction system cannula, single-use
Device class
Class I
Regulation number
872.6640
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental suction system cannula, single-use

Other devices from Plasdent Corp.

See all devices from Plasdent Corp. →

Properties

  • Single use
  • Premarket exempt
Other properties (13, all answered No)