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Tx™

FDA UDI

Class II (US FDA UDI)

by Innovasis, Inc.

Identity

Trade Name
Tx™ FDA UDI
Generic Name
Orthopaedic implant driver FDA UDI
Device Name
Al, Silicone, SST FDA UDI
Model / Reference
LS-395 FDA UDI
Description
Al, Silicone, SST FDA UDI

Identifiers

Primary DI / UDI-DI
M711LS3950 FDA UDI
510(k) Number
K180078 FDA UDI
FDA Product Code
MAX FDA UDI
GMDN Term
Orthopaedic implant driver FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3080 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic inorganic implant inserter/extractor, reusableOrthopaedic implant driver

Tx™ by Innovasis, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implant driver.

Cleared under the same submission

K180078 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Innovasis, Inc.

Sources (1)

  • FDA UDI 828a9fd6-a6bf-4aa8-8cac-8ca770ab6988 35 fields · synced Jun 8, 2026