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Truliant CC

FDA UDI

Class II (US FDA UDI)

by Exactech, Inc.

Identity

Trade Name
Truliant CC FDA UDI
Generic Name
Osteotomy guide, reusable FDA UDI
Device Name
TRULIANT CC NOTCH GUIDE, SIZE 5 FDA UDI
Model / Reference
02-019-10-0250 FDA UDI
Description
TRULIANT CC NOTCH GUIDE, SIZE 5 FDA UDI

Identifiers

Catalog Number
02-019-10-0250 FDA UDI
Primary DI / UDI-DI
10885862627339 FDA UDI
510(k) Number
K150890 FDA UDI
FDA Product Code
JWH FDA UDI
GMDN Term
Osteotomy guide, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3560 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Osteotomy guide, reusable

Truliant CC by Exactech, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Osteotomy 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
Exactech, Inc.

Sources (1)

  • FDA UDI bf57e533-7185-49c5-9ebb-b8d794f0376a 35 fields · synced May 30, 2026