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Ruthless Spine Duckbill Probe, Plastic RJB-FLT1

by Ruthless Spine

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 NumberG492RJBFLT10 UDI-DI Date9 Dec 2025ListedStatusListed 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  • Withdrawn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
Ruthless Spine Duckbill Probe, Plastic
Generic Name
Abdominal/ENT/orthopaedic surgical probe, single-use
Model / Ref / Catalog
RJB-FLT1, RJBFLT1
Primary DI / UDI-DI
G492RJBFLT10
510(k) Number
FDA Product Code
QWL
GMDN Term
Abdominal/ENT/orthopaedic surgical probe, single-use
Device Class
Class II
Regulation Number
888.4560
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K252615)

Other devices from Ruthless Spine

See all devices from Ruthless Spine →

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