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LxHA™

FDA UDI

Class II (US FDA UDI)

by Innovasis, Inc.

Identity

Trade Name
LxHA™ FDA UDI
Generic Name
Surgical mallet FDA UDI
Device Name
SST FDA UDI
Model / Reference
LS-479 FDA UDI
Description
SST FDA UDI

Identifiers

Catalog Number
LS-479 FDA UDI
Primary DI / UDI-DI
M711LS4790 FDA UDI
FDA Product Code
MAX FDA UDI
GMDN Term
Surgical mallet 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

Yes

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: Surgical mallet

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

Similar devices

Also classified as Surgical mallet.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Innovasis, Inc.

Sources (1)

  • FDA UDI e308b32e-32f4-4a80-82e4-5e6b6bcf84b3 35 fields · synced May 30, 2026