← Back to catalogue

Amber® Mill Direct

FDA UDI

Class II (US FDA UDI)

by Hass Corporation

Identity

Trade Name
Amber® Mill Direct FDA UDI
Generic Name
Dental appliance fabrication material, ceramic FDA UDI
Model / Reference
Amber Mill Direct MT C12/C1 FDA UDI

Identifiers

Primary DI / UDI-DI
08800057168614 FDA UDI
510(k) Number
K202952 FDA UDI
FDA Product Code
EIH FDA UDI
GMDN Term
Dental appliance fabrication material, ceramic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.6660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental appliance fabrication material, ceramic

Amber® Mill Direct by Hass Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, ceramic.

Cleared under the same submission

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
Hass Corporation

Sources (1)

  • FDA UDI bb516bfa-ae87-484d-84f5-0c313b691e02 33 fields · synced May 31, 2026