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Firebird Nxg Poct 36-1908

by Orthofix US LLC

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 Number18257200142576 UDI-DI Date17 Jul 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  • Withdrawn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
Firebird Nxg Poct
Generic Name
Abdominal/ENT/orthopaedic surgical probe, reusable
Model / Reference
36-1908
Primary DI / UDI-DI
18257200142576
510(k) Number
FDA Product Code
OLO
GMDN Term
Abdominal/ENT/orthopaedic surgical probe, reusable
Device Class
Class II
Regulation Number
882.4560
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K172115)

Show all (12)

Other devices from Orthofix US LLC

See all devices from Orthofix US LLC →

Properties

  • Prescription Use
  • Lot / Batch Number

Other properties (12)

  • 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
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No