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OIC External Fixation System

FDA UDI

Class II (US FDA UDI)

by Orthopaedic Implant Company, The

Identity

Trade Name
OIC External Fixation System FDA UDI
Generic Name
Orthopaedic implantation sleeve, reusable FDA UDI
Device Name
TISSUE PROTECTOR SLEEVE FDA UDI
Model / Reference
01-EXF02 FDA UDI
Description
TISSUE PROTECTOR SLEEVE FDA UDI

Identifiers

Primary DI / UDI-DI
M69601EXF020 FDA UDI
510(k) Number
K171211 FDA UDI
FDA Product Code
KTT FDA UDI
GMDN Term
Orthopaedic implantation sleeve, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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

Category: Orthopaedic implantation sleeve, reusable

OIC External Fixation System by Orthopaedic Implant Company, The — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implantation sleeve, reusable.

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 8f438fad-9c8f-49c5-8c5e-515f710b0d7c 35 fields · synced May 30, 2026