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Saberscope™ Video Processing Unit VPUX-1

by Xenocor, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00854490007052 UDI-DI Date20 Apr 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Saberscope™ Video Processing Unit
Generic Name
Endoscopic video image processing unit
Model / Ref / Catalog
VPUX-1
Primary DI / UDI-DI
00854490007052
510(k) Number
FDA Product Code
GCJ, HET, GCQ
GMDN Term
Endoscopic video image processing unit
Device Class
Class II
Regulation Number
876.1500, 884.1720
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K260177)

Other devices from Xenocor, Inc.

See all devices from Xenocor, Inc. →

Properties

  • Prescription Use
  • Lot / Batch Number
  • Serial Number
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Expiration Date: No