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Tearscience Activator Clear

FDA UDI

Class II (US FDA UDI)

by Johnson & Johnson Surgical Vision, Inc.

Identity

Trade Name
TEARSCIENCE ACTIVATOR CLEAR FDA UDI
Generic Name
Eyelid thermal pulsation system applicator, single-use FDA UDI
Device Name
TS ACTIVATOR CLEAR, BOX OF 10, US FDA UDI
Model / Reference
LFD-2100 FDA UDI
Description
TS ACTIVATOR CLEAR, BOX OF 10, US FDA UDI

Identifiers

Catalog Number
0803-5051 FDA UDI
Primary DI / UDI-DI
00810051250077 FDA UDI
FDA Product Code
ORZ FDA UDI
GMDN Term
Eyelid thermal pulsation system applicator, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.5200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Eyelid thermal pulsation system applicator, single-use

Tearscience Activator Clear by Johnson & Johnson Surgical Vision, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Eyelid thermal pulsation system applicator, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Johnson & Johnson Surgical Vision, Inc.

Sources (1)

  • FDA UDI a6ced1d1-5fb0-4157-a7a0-2ce6c84aaa20 35 fields · synced Jun 9, 2026