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Forest

FDA UDI

Class I (US FDA UDI)

by Ls Enterprises, Inc.

Identity

Trade Name
Forest FDA UDI
Generic Name
Dental delivery system FDA UDI
Device Name
ASST'S DELIVERY PRO 7000 SERIES, BENEATH COUNTER, FOREST GREY FDA UDI
Model / Reference
7022PRO-BC-G FDA UDI
Description
ASST'S DELIVERY PRO 7000 SERIES, BENEATH COUNTER, FOREST GREY FDA UDI

Identifiers

Primary DI / UDI-DI
D0697022PROBCG0 FDA UDI
510(k) Number
K173608 FDA UDI
FDA Product Code
EIA FDA UDI
GMDN Term
Dental delivery system 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

No

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental delivery system

Forest by Ls Enterprises, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental delivery system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 685c90c0-5f93-44ed-a49e-c510bf37bbe8 34 fields · synced May 31, 2026