Skip to content

ProneView D28621

by Dupaco, Inc.

ProneView D28621 is a Class I device made by Dupaco, Inc., listed in FDA GUDID since 30 Oct 2020 (UDI-DI 10850017419169), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10850017419169 UDI-DI Date30 Oct 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  • Withdrawn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
ProneView
Generic name
Freestanding patient positioner, single-use
Model / Ref / Catalog
D28621
Primary DI / UDI-DI
10850017419169
FDA product code
CCX
GMDN term
Freestanding patient positioner, single-use
Device class
Class I
Regulation number
868.6820
GUDID distribution status
In Commercial Distribution

Related devices

Category: Freestanding patient positioner, single-use

Similar devices

Other devices filed under FDA product code CCX (SUPPORT, PATIENT POSITION).

Other devices from Dupaco, Inc.

See all devices from Dupaco, Inc. →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)