Revolver Universal Connector

FDA UDI

Class II (US FDA UDI)

by Katalyst Surgical, Llc

Identity

Trade Name: Revolver Universal Connector FDA UDI
Generic Name: Light source adaptor FDA UDI
Device Name: Revolver Universal Connector FDA UDI
Model / Reference: RLP-A FDA UDI
Description: Revolver Universal Connector FDA UDI

Identifiers

Primary DI / UDI-DI: 00840096208276 FDA UDI
510(k) Number: K140362 FDA UDI
FDA Product Code: MPA FDA UDI
GMDN Term: Light source adaptor FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.1500 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

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Light source adaptor

Revolver Universal Connector by Katalyst Surgical, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Light source adaptor.

Aspen® Rigid Light Handle Adapter — Aspen Surgical Products, Inc. · Class II
Gyrus ACMI — Gyrus Acmi, Inc. · Class II
Aspen® Flexible Light Handle Adapter — Aspen Surgical Products, Inc. · Class II
Aspen® Flexible Light Handle Cover — Aspen Surgical Products, Inc. · Class II
Aspen® Flexible Light Handle Adapter — Aspen Surgical Products, Inc. · Class II
Innomed, Inc. — Innomed, Inc. · Class II
Aspen® Rigid Light Handle Adapter — Aspen Surgical Products, Inc. · Class II
SPOTLIGHT — Depuy Spine, Inc. · Class I

Cleared under the same submission

K140362 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: Katalyst Surgical, Llc

Sources (1)

FDA UDI 6eb30b8d-c4bd-40b4-b02d-bad6ca7be5a4 34 fields · synced May 30, 2026