Obsidian® Press Over Zirconia
K-Number: K262239 · 2026-07-30
Device Summary
Frequently Asked Questions
What is the Obsidian® Press Over Zirconia?
Obsidian® Press Over Zirconia is a medical device that received FDA 510(k) clearance on 2026-07-30. The listed applicant is Prismatik Dentalcraft, Inc.. The 510(k) number is K262239.
When did Obsidian® Press Over Zirconia receive FDA 510(k) clearance?
Obsidian® Press Over Zirconia received FDA 510(k) clearance on 2026-07-30, under 510(k) number K262239.
Who is the listed applicant for Obsidian® Press Over Zirconia?
The FDA 510(k) record lists Prismatik Dentalcraft, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Obsidian® Press Over Zirconia?
The FDA product code for Obsidian® Press Over Zirconia is EIH.
Other records listing Prismatik Dentalcraft, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: EIH)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.