Phasor

Phasor Cranial Access Kit, with Phasor Drill quick-connect, 6.35-mm Bit, with Phasor Legacy manual drill and Phasor electric Drill, with Kit

Registry build 21.09.26
2manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

All of them in Shanghai. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code HBG
Manufacturer City Province Registered as Device types
Shanghai Medical Instruments (Group) Ltd. Corp. Shanghai Shanghai Contract manufacturer 235
Shanghai Wilpower Industrial Co., Ltd. Shanghai Shanghai Exporter 33

Record

Regulatory record for Phasor
Listed by Phasor Health, LLC, United States
FDA product code HBG
Device type Drills, Burrs, Trephines & Accessories (Manual)
Device class Class 2
Regulation 21 CFR 882.4300
Establishment Specification developer, Complaint-file establishment, Manufacturer
Record published 2026-01-19
Record revised 2026-03-30 (version 2)

Specifications

Specifications
MRI safety MR Unsafe
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for Phasor
Catalogue number Size Status
6.35CK In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Integra® Ruggles®-Redmond™ Integra LifeSciences Production Corporation 508
Integra® Jarit® Integra LifeSciences Production Corporation 172
Integra® Miltex® Integra LifeSciences Production Corporation 65
Drills, Burrs, Trephines & Accessories (Manual) Synthes Gmbh 34
Integra® Integra Pain Management 7
Symmetry Surgical Aspen Surgical Products, Inc. 6
Symmetry Hudson Aspen Surgical Products, Inc. 5
Symmetry Cushing Aspen Surgical Products, Inc. 4
V. Mueller Steris Corporation 3
SmartTip ClearPoint Neuro Inc. 3
Drill Bit Neurovention, LLC 2
Codman® Integra LifeSciences Production Corporation 2

Showing 12 of 41. All products under Drills, Burrs, Trephines & Accessories (Manual)

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K252696 2025-11-21

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer