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Earlens Tympanic Lens

FDA UDI

Class II (US FDA UDI)

by Earlens Corporation

Identity

Trade Name
Earlens Tympanic Lens FDA UDI
Generic Name
Tympanic membrane contact hearing aid tympanic transducer FDA UDI
Device Name
Inductive Tympanic Lens L- left, R - Right FDA UDI
Model / Reference
ITL01X FDA UDI
Description
Inductive Tympanic Lens L- left, R - Right FDA UDI

Identifiers

Catalog Number
ITL01X FDA UDI
Primary DI / UDI-DI
00850013007240 FDA UDI
510(k) Number
K182480 FDA UDI
FDA Product Code
PLK FDA UDI
GMDN Term
Tympanic membrane contact hearing aid tympanic transducer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.3315 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Earlens Tympanic Lens by Earlens Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Earlens Corporation

Sources (1)

  • FDA UDI 9e35c62e-ace2-4607-a281-ef2dfde26e01 37 fields · synced Jun 6, 2026