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Euclid Orthokeratology (tisilfocon A) Contact Lenses for Overnight Wear

FDA UDI

Class III (US FDA UDI)

by Euclid Vision Corporation

Identity

Trade Name
Euclid Orthokeratology (tisilfocon A) Contact Lenses for Overnight Wear FDA UDI
Generic Name
Orthokeratology contact lens FDA UDI
Device Name
Emerald, tisilfocon A, Blue FDA UDI
Model / Reference
Emerald FDA UDI
Description
Emerald, tisilfocon A, Blue FDA UDI

Identifiers

Primary DI / UDI-DI
00850007135041 FDA UDI
FDA Product Code
NUU FDA UDI
GMDN Term
Orthokeratology contact lens FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
886.5916 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthokeratology contact lens

Euclid Orthokeratology (tisilfocon A) Contact Lenses for Overnight Wear by Euclid Vision Corporation — Class III — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Orthokeratology contact lens.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dcad5a0e-4beb-45f6-acad-5db893a98f4e 34 fields · synced May 30, 2026