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Halo Systems

FDA UDI

Class II (US FDA UDI)

by Ossur Americas

Identity

Trade Name
Halo Systems FDA UDI
Generic Name
Traction system skull tongs FDA UDI
Device Name
J TONG SML/MED- No App FDA UDI
Model / Reference
JT-215 FDA UDI
Description
J TONG SML/MED- No App FDA UDI

Identifiers

Catalog Number
JT-215 FDA UDI
Primary DI / UDI-DI
05690977308718 FDA UDI
510(k) Number
K930021 FDA UDI
FDA Product Code
HAX FDA UDI
GMDN Term
Traction system skull tongs FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5960 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI
MRI Safety
MR Conditional FDA UDI

Halo Systems by Ossur Americas — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ossur Americas

Sources (1)

  • FDA UDI cf5aa420-5cbe-447e-8c2f-f9fed4bc92c4 36 fields · synced Jun 7, 2026