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Excella®

FDA UDI

Class I (US FDA UDI)

by Innovasis, Inc.

Identity

Trade Name
Excella® FDA UDI
Generic Name
Spinal intraoperative positioning pin, reusable FDA UDI
Device Name
Pedicle Marker, Cone, Excella-P, SST FDA UDI
Model / Reference
LA-113 FDA UDI
Description
Pedicle Marker, Cone, Excella-P, SST FDA UDI

Identifiers

Primary DI / UDI-DI
M711LA1130 FDA UDI
FDA Product Code
HXB FDA UDI
GMDN Term
Spinal intraoperative positioning pin, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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: Spinal intraoperative positioning pin, reusable

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

Similar devices

Also classified as Spinal intraoperative positioning pin, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Innovasis, Inc.

Sources (1)

  • FDA UDI 6ebd9d5a-599f-4ddd-8eb0-e8c1c5179906 34 fields · synced Jun 8, 2026