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Scancoat 305-SCB

by Domico Med-Device, LLC

Scancoat 305-SCB is a Class I device made by Domico Med-Device, LLC, listed in FDA GUDID since 11 Aug 2022 (UDI-DI 00810050245388), 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 Number00810050245388 UDI-DI Date11 Aug 2022ListedStatusListed 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  • Withdrawn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
Scancoat
Generic name
Multifunction body cushion
Model / reference
305-SCB
Primary DI / UDI-DI
00810050245388
FDA product code
CCX
GMDN term
Multifunction body cushion
Device class
Class I
Regulation number
868.6820
GUDID distribution status
In Commercial Distribution

Related devices

Category: Multifunction body cushion

Similar devices in this category

Other devices filed under Multifunction body cushion.

Other devices from Domico Med-Device, LLC

See all devices from Domico Med-Device, LLC →

Properties

  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)