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PASCAL Synthesis, 532nm

FDA UDI

Class II (US FDA UDI)

by Iridex Corporation

Identity

Trade Name
PASCAL Synthesis, 532nm FDA UDI
Generic Name
Ophthalmic solid-state laser system, photodisruption FDA UDI
Device Name
Synthesis III, SLC AND ESF (532nm) D7 - IRIDEX FDA UDI
Model / Reference
PASCAL Synthesis 532 FDA UDI
Description
Synthesis III, SLC AND ESF (532nm) D7 - IRIDEX FDA UDI

Identifiers

Catalog Number
SA-06414 FDA UDI
Primary DI / UDI-DI
00813125016760 FDA UDI
510(k) Number
K123542 FDA UDI
FDA Product Code
HQF FDA UDI
GEX FDA UDI
GMDN Term
Ophthalmic solid-state laser system, photodisruption FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4390 FDA UDI
878.4810 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

Category: Ophthalmic solid-state laser system, photodisruption

PASCAL Synthesis, 532nm by Iridex Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic solid-state laser system, photodisruption.

Cleared under the same submission

K123542 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Iridex Corporation

Sources (1)

  • FDA UDI 87979ecd-1b0a-4d7f-932a-fd576d63e195 37 fields · synced Jun 9, 2026