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Earlens Tympanic Lens, Left

FDA UDI

Class II (US FDA UDI)

by Earlens Corporation

Identity

Trade Name
Earlens Tympanic Lens, Left FDA UDI
Generic Name
Tympanic membrane contact hearing aid tympanic transducer FDA UDI
Model / Reference
ITL01L FDA UDI

Identifiers

Catalog Number
ITL01L FDA UDI
Primary DI / UDI-DI
00850013007561 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
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

Category: Tympanic membrane contact hearing aid tympanic transducer

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

Similar devices

Also classified as Tympanic membrane contact hearing aid tympanic transducer.

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 c032a99b-a0c3-46f6-a110-6f0444e223dd 35 fields · synced Jun 8, 2026