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THUNDERBEAT 5 mm, 20 cm, Front-actuated Grip Type S TB-0520FCS

by Olympus Medical Systems Corporation 2 variants

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 Number04953170475009 UDI-DI Date5 Oct 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  • Withdrawn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
THUNDERBEAT 5 mm,20 cm,Front-actuated Grip Type S
Generic Name
Endoscopic electrosurgical/ultrasonic surgical system instrument
Model / Ref / Catalog
TB-0520FCS, N5424041
Primary DI / UDI-DI
04953170475009
510(k) Number
FDA Product Code
GEI, LFL
GMDN Term
Endoscopic electrosurgical/ultrasonic surgical system instrument
Device Class
Class II
Regulation Number
878.4400
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Related devices

Cleared under the same submission (K254056)

Other devices from Olympus Medical Systems Corporation

See all devices from Olympus Medical Systems Corporation →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

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