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PENTAX Medical VNL11-J10

by Hoya Corporation 4 variants

Listed FDA GUDID listing, not in commercial distribution

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 Number04961333251155 UDI-DI Date2 Feb 2022ListedStatusListed GUDID: not 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  • Withdrawn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
PENTAX Medical
Generic Name
Flexible video otorhinolaryngoscope, reusable
Model / Reference
VNL11-J10
Primary DI / UDI-DI
04961333251155
FDA Product Code
EOB
GMDN Term
Flexible video otorhinolaryngoscope, reusable
Device Class
Class II
Regulation Number
874.4760
GUDID distribution status
Not in Commercial Distribution

Related devices

Cleared under the same submission (K172156)

Show all (12)

Other devices from Hoya Corporation

See all devices from Hoya Corporation →

Properties

  • Prescription Use
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • 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
  • Lot / Batch Number: No
  • Expiration Date: No