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X-Pac

FDA UDI

Class II (US FDA UDI)

by Expanding Innovations, Inc.

Identity

Trade Name
X-PAC FDA UDI
Generic Name
General internal orthopaedic fixation system implantation kit FDA UDI
Device Name
Adjustable Awl FDA UDI
Model / Reference
EI3210 FDA UDI
Description
Adjustable Awl FDA UDI

Identifiers

Catalog Number
EI3210 FDA UDI
Primary DI / UDI-DI
00850041805528 FDA UDI
510(k) Number
K250602 FDA UDI
FDA Product Code
KWQ FDA UDI
GMDN Term
General internal orthopaedic fixation system implantation kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: General internal orthopaedic fixation system implantation kit

X-Pac by Expanding Innovations, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General internal orthopaedic fixation system implantation kit.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cd3bbfa7-51f1-49d8-be3f-ad011f818a7f 36 fields · synced May 30, 2026