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Excella MIS®

FDA UDI

Class II (US FDA UDI)

by Innovasis, Inc.

Identity

Trade Name
Excella MIS® FDA UDI
Generic Name
Orthopaedic bone wire FDA UDI
Device Name
Nitinol FDA UDI
Model / Reference
LS-568 FDA UDI
Description
Nitinol FDA UDI

Identifiers

Primary DI / UDI-DI
M711LS5680 FDA UDI
510(k) Number
K102248 FDA UDI
FDA Product Code
NKB FDA UDI
MNI FDA UDI
MNH FDA UDI
KWP FDA UDI
KWQ FDA UDI
GMDN Term
Orthopaedic bone wire FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 FDA UDI
888.3050 FDA UDI
888.3060 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Dimensions & Sizes

Size
Length — 500 Millimeter FDA UDI
Outer Diameter — 1.4 Millimeter FDA UDI

Category: Orthopaedic bone wire

Excella MIS® by Innovasis, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone wire.

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 8b10d85e-f43b-42d5-ae19-422d30800ae3 36 fields · synced Jun 6, 2026