Surgify Halo | 5.4 Mm | Extendable

2 catalogue numbers from 54.000.SEE.U1, listed by Surgify Medical OY, Finland, under Drills, Burrs, Trephines & Accessories (Simple, Powered). 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
2catalogue numbers in this listing
4510(k) clearances naming this product code
19recalls on this code

Who Else Makes It

Concentrated in Jiangsu (2), Shanghai (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HBE
Manufacturer City Province Registered as Device types
Shanghai Medical Instruments (Group) Ltd. Corp. Shanghai Shanghai Contract manufacturer 235
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53

Record

Regulatory record for Surgify Halo | 5.4 mm | Extendable
Listed by Surgify Medical OY, Finland
FDA product code HBE
Device type Drills, Burrs, Trephines & Accessories (Simple, Powered)
Device class Class 2
Regulation 21 CFR 882.4310
Establishment Manufacturer
Record published 2026-03-31

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Surgify Halo | 5.4 mm | Extendable
Catalogue number Size Status
54.000.SEE.U1 In distribution
54.000.SEE.H1 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Midas REX MR8 Medtronic Powered Surgical Solutions 1,006
Drills, Burrs, Trephines & Accessories (Simple, Powered) Stryker GmbH 948
Elan 4 Aesculap AG 529
Drills, Burrs, Trephines & Accessories (Simple, Powered) Synthes Gmbh 514
Zethon Zethon Ltd 237
Drills, Burrs, Trephines & Accessories (Simple, Powered) Stryker Leibinger Gmbh & Co. KG 220
Midas Rex® Medtronic Powered Surgical Solutions 167
HiCUT Burs Adeor Medical AG 90
Phasor Phasor Health, LLC 80
Traumaone System Biomet Microfixation 62
Midas REX Microsaws Medtronic Powered Surgical Solutions 60
Mids REX MR8 Medtronic Powered Surgical Solutions 59

Showing 12 of 269. All products under Drills, Burrs, Trephines & Accessories (Simple, Powered)

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K253627 2026-03-26
K251433 2025-06-04
K250380 2025-03-13
K232684 2023-11-29

Recalls Naming This Product

2 recalls name this product by its own identifiers, the UDI on its label.

Recalls naming the identifiers of Surgify Halo | 5.4 mm | Extendable
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Surgify Medical OY UDI-DI 2026-04-30 Class II Under Investigation by firm Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). 53 units
Surgify Medical OY UDI-DI 2026-04-30 Class II Under Investigation by firm Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). 8 units

Recalls

17 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity
2026-04-30 Class II Under Investigation by firm Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30 Class II Under Investigation by firm Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30 Class II Under Investigation by firm Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). 0
2026-04-30 Class II Under Investigation by firm Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30 Class II Under Investigation by firm Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30 Class II Under Investigation by firm Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30 Class II Under Investigation by firm Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30 Class II Under Investigation by firm Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30 Class II Under Investigation by firm Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30 Class II Under Investigation by firm Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). 112 units
2026-04-30 Class II Under Investigation by firm Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30 Class II Under Investigation by firm Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). 15 units
2026-04-30 Class II Under Investigation by firm Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30 Class II Under Investigation by firm Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30 Class II Under Investigation by firm Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30 Class II Under Investigation by firm Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). 0
2026-04-30 Class II Under Investigation by firm Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).

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