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In Touch Sterile Lancets

FDA UDI

Class II (US FDA UDI)

by Livongo Health, Inc

Identity

Trade Name
In Touch Sterile Lancets FDA UDI
Generic Name
Blood lancing device tip FDA UDI
Device Name
Box of 100 Sterile Lancets FDA UDI
Model / Reference
In Touch FDA UDI
Description
Box of 100 Sterile Lancets FDA UDI

Identifiers

Catalog Number
OFG00142 FDA UDI
Primary DI / UDI-DI
00853553005066 FDA UDI
510(k) Number
K133584 FDA UDI
FDA Product Code
FMK FDA UDI
GMDN Term
Blood lancing device tip FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4850 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

In Touch Sterile Lancets by Livongo Health, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K133584 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Livongo Health, Inc

Sources (1)

  • FDA UDI 1bc1fc3b-e86a-4d89-81a3-cdaecb1d2530 37 fields · synced Jun 1, 2026