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AMA Optics Panoramic Pinhole

FDA UDI

Class I (US FDA UDI)

by AMA Optics, Inc.

Identity

Trade Name
AMA Optics Panoramic Pinhole FDA UDI
Generic Name
Trial lens FDA UDI
Device Name
An individual ophthalmic lens from a trial lens set having multiple pinholes separate by clear plastic. FDA UDI
Model / Reference
PH-01-PH FDA UDI
Description
An individual ophthalmic lens from a trial lens set having multiple pinholes separate by clear plastic. FDA UDI

Identifiers

Catalog Number
PH01 FDA UDI
Primary DI / UDI-DI
G506PH010 FDA UDI
FDA Product Code
HPB FDA UDI
GMDN Term
Trial lens FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1410 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Trial lens

AMA Optics Panoramic Pinhole by AMA Optics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Trial lens.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
AMA Optics, Inc.

Sources (1)

  • FDA UDI 898a9b22-d7b9-45c1-8a90-4b81e1bec84c 34 fields · synced May 30, 2026