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Hexa

FDA UDI

Class II (US FDA UDI)

by Hexa Dental

Identity

Trade Name
Hexa FDA UDI
Generic Name
Dental etching solution FDA UDI
Device Name
DentalEtching Get FDA UDI
Model / Reference
HE-1050 FDA UDI
Description
DentalEtching Get FDA UDI

Identifiers

Catalog Number
HE-1050 FDA UDI
Primary DI / UDI-DI
00850023750006 FDA UDI
510(k) Number
K982191 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Dental etching solution FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3690 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental etching solution

Hexa by Hexa Dental — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental etching solution.

Cleared under the same submission

K982191 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hexa Dental

Sources (1)

  • FDA UDI cee68232-b301-4ef0-9d72-1c4869a5946d 36 fields · synced May 30, 2026