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Drape KB100 Series KB100DAB

by Kent Imaging Inc

Drape KB100 Series KB100DAB is a Class II device made by Kent Imaging Inc, listed in FDA GUDID since 21 Jul 2026 (UDI-DI B376KB100DAB0), 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 NumberB376KB100DAB0 UDI-DI Date21 Jul 2026ListedStatusListed 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  • Withdrawn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
Drape KB100 Series
Generic name
Patient surgical drape, single-use
Model / reference
KB100DAB
Primary DI / UDI-DI
B376KB100DAB0
FDA product code
PUI
GMDN term
Patient surgical drape, single-use
Device class
Class II
Regulation number
878.4370
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code PUI (Drape, Surgical, Exempt).

Other devices from Kent Imaging Inc

See all devices from Kent Imaging Inc →

Properties

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