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Truliant®

FDA UDI

Class II (US FDA UDI)

by Exactech, Inc.

Identity

Trade Name
TRULIANT® FDA UDI
Generic Name
Trabeculated knee tibia/insert prosthesis FDA UDI
Device Name
Porous Tibial Tray without Screw Holes FDA UDI
Model / Reference
02-022-56-4045 FDA UDI
Description
Porous Tibial Tray without Screw Holes FDA UDI

Identifiers

Catalog Number
02-022-56-4045 FDA UDI
Primary DI / UDI-DI
10885862608185 FDA UDI
510(k) Number
K240393 FDA UDI
FDA Product Code
MBH FDA UDI
JWH FDA UDI
GMDN Term
Trabeculated knee tibia/insert prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3565 FDA UDI
888.3560 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Trabeculated knee tibia/insert prosthesis

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

Similar devices

Also classified as Trabeculated knee tibia/insert prosthesis.

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 dbacb1eb-4435-49c5-8b1d-8a6ae61a0f84 36 fields · synced May 31, 2026