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Inion FreedomPin Instruments

FDA UDI

Class I (US FDA UDI)

by Inion , Ltd.

Identity

Trade Name
Inion FreedomPin Instruments FDA UDI
Generic Name
Bone tack inserter, basic FDA UDI
Device Name
Applicator 1.5 mm FDA UDI
Model / Reference
2 FDA UDI
Description
Applicator 1.5 mm FDA UDI

Identifiers

Catalog Number
INS-9280 FDA UDI
Primary DI / UDI-DI
06438408007293 FDA UDI
FDA Product Code
HXJ FDA UDI
GMDN Term
Bone tack inserter, basic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone tack inserter, basic

Inion FreedomPin Instruments by Inion , Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone tack inserter, basic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Inion , Ltd.

Sources (1)

  • FDA UDI d184781a-df61-4e92-8593-de2901640899 34 fields · synced May 30, 2026