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Phasor 2-In-1-05CK

by Phasor Health, LLC

Phasor 2-In-1-05CK is a Class II device made by Phasor Health, LLC, listed in FDA GUDID since 27 Mar 2026 (UDI-DI B7752IN105CK0), 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 NumberB7752IN105CK0 UDI-DI Date27 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  • Withdrawn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
2-IN-1-05CK
Primary DI / UDI-DI
B7752IN105CK0
FDA product code
HBE, OJG, HBG
GMDN term
Cranial trephine, single-use
Device class
Class II
Regulation number
882.4310, 882.4525, 882.4300
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

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Properties

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