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Anovo Instrument ARM Curved Scissors FP-01-0005

by Momentis Surgical Ltd

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 Number17290018151348 UDI-DI Date6 Apr 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  • Withdrawn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
Anovo Instrument ARM Curved Scissors
Generic Name
Robotic endoscopic electrosurgical instrument, bipolar/monopolar
Catalog Number
FP-01-0005
Primary DI / UDI-DI
17290018151348
510(k) Number
FDA Product Code
QNM
GMDN Term
Robotic endoscopic electrosurgical instrument, bipolar/monopolar
Device Class
Class II
Regulation Number
878.4961
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K243182)

Cleared under the same submission (K251056)

Cleared under the same submission (K251761)

Other devices from Momentis Surgical Ltd

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • 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