← Back to catalogue

Earlens Processor & Ear Tip

FDA UDI

Class II (US FDA UDI)

by Earlens Corporation

Identity

Trade Name
Earlens Processor & Ear Tip FDA UDI
Generic Name
Tympanic membrane contact hearing aid sound processor FDA UDI
Device Name
Kit containing 1 Processor and 1 LIght Tip that are connected together Processor comes in different colors: CH - Champagne, SI - Sliver, BL - Black, Ear Tip comes in L - Left, R - Right FDA UDI
Model / Reference
PET01X FDA UDI
Description
Kit containing 1 Processor and 1 LIght Tip that are connected together Processor comes in different colors: CH - Champagne, SI - Sliver, BL - Black, Ear Tip comes in L - Left, R - Right FDA UDI

Identifiers

Catalog Number
PET01X FDA UDI
Primary DI / UDI-DI
00850013007233 FDA UDI
510(k) Number
K182480 FDA UDI
FDA Product Code
PLK FDA UDI
GMDN Term
Tympanic membrane contact hearing aid sound processor 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

Yes

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

Earlens Processor & Ear Tip 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Earlens Corporation

Sources (1)

  • FDA UDI 25859da4-bc42-46f1-be82-e2f3a9b9abd9 37 fields · synced May 30, 2026