Amplivox

FDA UDI

Class II (US FDA UDI)

by Amplivox, Ltd.

Identity

Trade Name: Amplivox FDA UDI
Generic Name: Impedance audiometer FDA UDI
Model / Reference: Otowave 302 FDA UDI

Identifiers

Primary DI / UDI-DI: 05060488901386 FDA UDI
510(k) Number: K171265 FDA UDI
FDA Product Code: ETY FDA UDI
NAS FDA UDI
GMDN Term: Impedance audiometer FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 874.1090 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

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

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Impedance audiometer

Amplivox by Amplivox, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Impedance audiometer.

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Silicone Ear Tips — Natus Medical Denmark ApS · Class I
1096 Madsen Zodiac Quick Check Probe Gen 2 — Natus Medical Denmark ApS · Class IIa
GN Otometrics A/S — Natus Medical Denmark ApS · Class II
Welch Allyn, Inc. — Welch Allyn, Inc. · Class II
VIOLA — INVENTIS SRL · Class II
Silicone Ear Tips — Natus Medical Denmark ApS · Class I

Cleared under the same submission

K171265 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: Amplivox, Ltd.

Sources (1)

FDA UDI ad5b17bb-4b7e-4083-81c8-f924fc62f674 33 fields · synced Jun 8, 2026