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Phasor 4-In-1-2456K

by Phasor Health, LLC

Phasor 4-In-1-2456K is a Class II device made by Phasor Health, LLC, listed in FDA GUDID since 28 Mar 2026 (UDI-DI B7754IN12456K0), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB7754IN12456K0 UDI-DI Date28 Mar 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Phasor
Generic name
Cranial trephine, single-use
Model / reference
4-IN-1-2456K
Primary DI / UDI-DI
B7754IN12456K0
FDA product code
HBE, OJG
GMDN term
Cranial trephine, single-use
Device class
Class II
Regulation number
882.4310, 882.4525
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

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See all devices from Phasor Health, LLC →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)