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Purzir

FDA UDI

Class II (US FDA UDI)

by Seattle Bioceramics, Inc.

Identity

Trade Name
Purzir FDA UDI
Generic Name
Dental appliance fabrication material, ceramic FDA UDI
Device Name
Purzir Dental Zirconia Blank FDA UDI
Model / Reference
HT A1 98-14 FDA UDI
Description
Purzir Dental Zirconia Blank FDA UDI

Identifiers

Primary DI / UDI-DI
00810087760298 FDA UDI
510(k) Number
K193055 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental appliance fabrication material, ceramic

Purzir by Seattle Bioceramics, Inc. — 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

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Manufacturer

Sources (1)

  • FDA UDI 9e43e30a-bc3a-4df6-9dad-323c440f3468 34 fields · synced Jun 8, 2026