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OptoMonitor OpM-bedrail post clamp

by Opsens

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07540184020072 UDI-DI Date30 Sep 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
OptoMonitor
Generic Name
Image display monitor mount
Model / Ref / Catalog
OpM-bedrail post clamp, F202007
Primary DI / UDI-DI
07540184020072
510(k) Number
FDA Product Code
DQX, DXO
GMDN Term
Image display monitor mount
Device Class
Class II
Regulation Number
870.1330, 870.2870
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K142598)

Show all (10)

Other devices from Opsens

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Properties

  • Lot / Batch Number

Other properties (13)

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