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Loop™

FDA UDI

Class II (US FDA UDI)

by Garrison Dental Solutions, L.l.c.

Identity

Trade Name
LOOP™ FDA UDI
Generic Name
Dental/surgical polymerization lamp FDA UDI
Device Name
LOOP™ LED Curing Light Handpiece FDA UDI
Model / Reference
CLA01 FDA UDI
Description
LOOP™ LED Curing Light Handpiece FDA UDI

Identifiers

Catalog Number
CLA01 FDA UDI
Primary DI / UDI-DI
00810038093628 FDA UDI
FDA Product Code
EBZ FDA UDI
GMDN Term
Dental/surgical polymerization lamp FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.6070 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
High-level Disinfectant FDA UDI

Category: Dental/surgical polymerization lamp

Loop™ by Garrison Dental Solutions, L.l.c. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental/surgical polymerization lamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 24d01e53-4801-482c-a1da-97abe3acae8d 35 fields · synced Jun 8, 2026