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Excella II®

FDA UDI

Class II (US FDA UDI)

by Innovasis, Inc.

Identity

Trade Name
Excella II® FDA UDI
Generic Name
Orthopaedic implant driver FDA UDI
Device Name
SST FDA UDI
Model / Reference
LS-129 FDA UDI
Description
SST FDA UDI

Identifiers

Catalog Number
LS-129 FDA UDI
Primary DI / UDI-DI
M711LS1290 FDA UDI
510(k) Number
K102248 FDA UDI
FDA Product Code
KWQ FDA UDI
KWP FDA UDI
MNH FDA UDI
MNI FDA UDI
NKB FDA UDI
GMDN Term
Orthopaedic implant driver FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 FDA UDI
888.3050 FDA UDI
888.3070 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 implant driver

Excella II® 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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Innovasis, Inc.

Sources (1)

  • FDA UDI dbe89042-7fb1-43bb-8a64-c8a2a9777300 36 fields · synced Jun 8, 2026