← Back to catalogue

Inion instrument

FDA UDI

Class II (US FDA UDI)

by Inion , Ltd.

Identity

Trade Name
Inion instrument FDA UDI
Generic Name
Fluted surgical drill bit, reusable FDA UDI
Device Name
2.0 mm self tapping drill bit (AO-bayonet) FDA UDI
Model / Reference
0 FDA UDI
Description
2.0 mm self tapping drill bit (AO-bayonet) FDA UDI

Identifiers

Catalog Number
INS-9097 FDA UDI
Primary DI / UDI-DI
M224INS90979 FDA UDI
510(k) Number
K023887 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Fluted surgical drill bit, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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

K023887 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Inion , Ltd.

Sources (1)

  • FDA UDI 32feb04d-dfdf-4f4c-8818-dad121e0e1cf 36 fields · synced Jun 1, 2026