← Back to catalogue

Lateral Stopper

FDA UDI

Class I (US FDA UDI)

by Dentis Co. , Ltd

Identity

Trade Name
Lateral Stopper FDA UDI
Generic Name
Endodontic stopper FDA UDI
Device Name
Dental Implant Instrument / Lateral Stopper FDA UDI
Model / Reference
DSSLS30 FDA UDI
Description
Dental Implant Instrument / Lateral Stopper FDA UDI

Identifiers

Primary DI / UDI-DI
08806169146106 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Endodontic stopper FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Endodontic stopper

Lateral Stopper by Dentis Co. , Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endodontic stopper.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Dentis Co. , Ltd

Sources (1)

  • FDA UDI c5492e2b-50ee-40a0-b3c0-5702a36a76cb 33 fields · synced May 30, 2026