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Bio-LCB

FDA UDI

Class I (US FDA UDI)

by Essential Dental Systems, Inc.

Identity

Trade Name
Bio-LCB FDA UDI
Generic Name
Dental material injection cannula, single-use FDA UDI
Device Name
50 Light Cured Base and Liner Syringe Tips FDA UDI
Model / Reference
910-50 FDA UDI
Description
50 Light Cured Base and Liner Syringe Tips FDA UDI

Identifiers

Catalog Number
910-50 FDA UDI
Primary DI / UDI-DI
00766054002925 FDA UDI
FDA Product Code
EIY FDA UDI
GMDN Term
Dental material injection cannula, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental material injection cannula, single-use

Bio-LCB by Essential Dental Systems, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental material injection cannula, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a8ec5b1f-57b8-4031-9961-e545ecb7d020 36 fields · synced May 30, 2026