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CoLink

FDA UDI

Class I (US FDA UDI)

by In2Bones, USA

Identity

Trade Name
CoLink FDA UDI
Generic Name
Surgical drill guide, reusable FDA UDI
Device Name
MIS PLATE TARGETING GUIDE, KWIRE GUIDE FDA UDI
Model / Reference
P02 N0231 FDA UDI
Description
MIS PLATE TARGETING GUIDE, KWIRE GUIDE FDA UDI

Identifiers

Catalog Number
P02 N0231 FDA UDI
Primary DI / UDI-DI
00810021869827 FDA UDI
510(k) Number
K213069 FDA UDI
FDA Product Code
FZX FDA UDI
GMDN Term
Surgical drill guide, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

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
MRI Safety
MR Safe FDA UDI

Category: Surgical drill guide, reusable

CoLink by In2Bones, USA — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical drill guide, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
In2Bones, USA

Sources (1)

  • FDA UDI 8e578fa4-a231-4f40-975b-d71287a319a9 36 fields · synced May 30, 2026