StimSite

FDA UDI

Class II (US FDA UDI)

by Allotrope Medical, Inc.

Identity

Trade Name: StimSite FDA UDI
Generic Name: Nerve-locating system FDA UDI
Device Name: StimSite Ligasure Adapter FDA UDI
Model / Reference: AM-LS1 FDA UDI
Description: StimSite Ligasure Adapter FDA UDI

Identifiers

Catalog Number: AM-LS1 FDA UDI
Primary DI / UDI-DI: 00860002926940 FDA UDI
510(k) Number: K200886 FDA UDI
FDA Product Code: ETN FDA UDI
GMDN Term: Nerve-locating system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 874.1820 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Nerve-locating system

StimSite by Allotrope Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Nerve-locating system.

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AVANOS — Avanos Medical, Inc. · Class II
NIM-ECLIPSE® — MEDTRONIC XOMED, INC. · Class II
NIM-Eclipse® — MEDTRONIC XOMED, INC. · Class II
SENTIO — Medos International Sàrl · Class II
Halyard — Avanos Medical, Inc. · Class II

Cleared under the same submission

K200886 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Allotrope Medical, Inc.

Sources (1)

FDA UDI 769ca791-21b4-4b53-8eb7-274b98be7cf8 35 fields · synced Jun 8, 2026