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Onyx Saliva Ejectors

FDA UDI

Class I (US FDA UDI)

by Practicon, Inc.

Identity

Trade Name
Onyx Saliva Ejectors FDA UDI
Generic Name
Dental suction system cannula, single-use FDA UDI
Device Name
black saliva ejectors FDA UDI
Model / Reference
7158213 FDA UDI
Description
black saliva ejectors FDA UDI

Identifiers

Catalog Number
7158213 FDA UDI
Primary DI / UDI-DI
00723896019580 FDA UDI
FDA Product Code
DYN FDA UDI
GMDN Term
Dental suction system cannula, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6640 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental suction system cannula, single-use

Onyx Saliva Ejectors by Practicon, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental suction system cannula, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Practicon, Inc.

Sources (1)

  • FDA UDI b67f625a-51d8-40cc-98b7-4e923a73e73f 34 fields · synced May 31, 2026