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Corneal Shield

FDA UDI

Class I (US FDA UDI)

by Cynosure, LLC

Identity

Trade Name
CORNEAL SHIELD FDA UDI
Generic Name
Epithelial-resurfacing corneal shield FDA UDI
Device Name
CORNEAL SHIELD S(RED),4 SHIELDS,1 HANDLE FDA UDI
Model / Reference
H75A FDA UDI
Description
CORNEAL SHIELD S(RED),4 SHIELDS,1 HANDLE FDA UDI

Identifiers

Catalog Number
H75A FDA UDI
Primary DI / UDI-DI
00841494102395 FDA UDI
FDA Product Code
HOY FDA UDI
GMDN Term
Epithelial-resurfacing corneal shield FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4750 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Epithelial-resurfacing corneal shield

Corneal Shield by Cynosure, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Epithelial-resurfacing corneal shield.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cynosure, LLC

Sources (1)

  • FDA UDI ddd23262-54a6-42b2-aace-fe67785c8e11 34 fields · synced May 30, 2026