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InPulse Dental Laser

FDA UDI

Class II (US FDA UDI)

by Beyond International Inc.

Identity

Trade Name
InPulse Dental Laser FDA UDI
Generic Name
Dental solid-state laser system FDA UDI
Model / Reference
InPulse Touch 100 FDA UDI

Identifiers

Primary DI / UDI-DI
00857848007674 FDA UDI
FDA Product Code
GEX FDA UDI
GMDN Term
Dental solid-state laser system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 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

Yes

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 solid-state laser system

InPulse Dental Laser by Beyond International Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental solid-state laser system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9c05a46b-8e32-45b9-9de4-6139adf82389 32 fields · synced Jun 9, 2026