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Inion instrument

FDA UDI

Class II (US FDA UDI)

by Inion , Ltd.

Identity

Trade Name
Inion instrument FDA UDI
Generic Name
Bone tap, reusable FDA UDI
Device Name
3.1 mm bone tap with 42 mm stop FDA UDI
Model / Reference
0 FDA UDI
Description
3.1 mm bone tap with 42 mm stop FDA UDI

Identifiers

Catalog Number
INS-9063 FDA UDI
Primary DI / UDI-DI
M224INS90639 FDA UDI
510(k) Number
K010352 FDA UDI
FDA Product Code
JEY FDA UDI
GMDN Term
Bone tap, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4760 FDA UDI
Commercial Distribution
Not 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

No

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

Inion instrument by Inion , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K010352 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Inion , Ltd.

Sources (1)

  • FDA UDI 51821ffb-a92d-4b3f-9fd6-b38d2a16a38a 36 fields · synced May 30, 2026