How many FDA actions has Prismatik Dentalcraft, Inc. had?

Argus HQ has recorded 1 FDA events for Prismatik Dentalcraft, Inc.: 0 warning letters, 1 recalls, 0 approvals, and 0 Form 483 inspection observations. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.

What is the most recent FDA action against Prismatik Dentalcraft, Inc.?

The most recent FDA event Argus HQ has on file for Prismatik Dentalcraft, Inc. is dated 2026-07-29, with a severity rating of "high" in Argus HQ's classification. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.

Does Argus HQ track new FDA actions for Prismatik Dentalcraft, Inc. automatically?

Yes. Argus HQ ingests FDA sources daily, including FDA warning letters, recalls, drug and biologic approvals, and Form 483 inspection observations. When a new FDA action linked to Prismatik Dentalcraft, Inc. is observed, this page's event count and history update automatically.

How many FDA actions does Argus HQ track for Prismatik Dentalcraft, Inc.?

1 total: 0 warning letters, 1 recall, 0 approval records, and 0 Form 483 inspection citations.

Regulatory Record: Prismatik Dentalcraft, Inc.

FDA action counts

Total FDA actions	1
Warning letters	0
Recalls	1
Approval records	0
Form 483 inspection citations	0
Most recent action	July 29, 2026

Key takeaway: Argus HQ has recorded 1 FDA events for Prismatik Dentalcraft, Inc.: 0 warning letters, 1 recalls, 0 approvals, and 0 inspection 483 observations. These events span from 2026-07-29 to 2026-07-29. The most severe rating Argus HQ has assigned across this history is "high". Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed.

Risk pattern analysis

Argus HQ analysis — not an FDA finding

This section is Argus HQ analysis, not an FDA finding. Prismatik Dentalcraft, Inc. has 1 FDA event on file. A pattern across multiple FDA touchpoints does not by itself establish that any specific product currently poses a risk; it reflects only the frequency of FDA engagement with this company as recorded in Argus HQ's database. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed. Argus HQ does not independently verify FDA's underlying findings; this page summarizes what FDA has published and links back to the original FDA source for each event. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.

Enforcement history

On 2026-07-29, Argus HQ recorded an FDA recall for Prismatik Dentalcraft, Inc., rated "high" severity in Argus HQ's classification: Prismatik Dentalcraft, Inc. — Class II recall: Brand Name: Silent Nite Product Name: Silent Nite Sleep Appliance Model/Cata…. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed.

Frequently asked questions

How many FDA actions has Prismatik Dentalcraft, Inc. had?: Argus HQ has recorded 1 FDA events for Prismatik Dentalcraft, Inc.: 0 warning letters, 1 recalls, 0 approvals, and 0 Form 483 inspection observations. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.
What is the most recent FDA action against Prismatik Dentalcraft, Inc.?: The most recent FDA event Argus HQ has on file for Prismatik Dentalcraft, Inc. is dated 2026-07-29, with a severity rating of "high" in Argus HQ's classification. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.
Does Argus HQ track new FDA actions for Prismatik Dentalcraft, Inc. automatically?: Yes. Argus HQ ingests FDA sources daily, including FDA warning letters, recalls, drug and biologic approvals, and Form 483 inspection observations. When a new FDA action linked to Prismatik Dentalcraft, Inc. is observed, this page's event count and history update automatically.
How many FDA actions does Argus HQ track for Prismatik Dentalcraft, Inc.?: 1 total: 0 warning letters, 1 recall, 0 approval records, and 0 Form 483 inspection citations.

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Prismatik Dentalcraft, Inc. — Class II recall: Brand Name: Silent Nite Product Name: Silent Nite Sleep Appliance Model/Cata… →

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Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder

Verified from FDA.gov · Last updated: Jul 29, 2026

Cite this record

Reusing this data in reporting or research? Here’s a ready-made citation.

APA

Argus HQ Research (2026). Regulatory Record: Prismatik Dentalcraft, Inc.. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/company/prismatik-dentalcraft-inc

MLA

"Regulatory Record: Prismatik Dentalcraft, Inc.." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/company/prismatik-dentalcraft-inc.

Chicago

Argus HQ Research. "Regulatory Record: Prismatik Dentalcraft, Inc.." Digital Empire Holdings LLC. Accessed August 4, 2026. https://argushq.ai/company/prismatik-dentalcraft-inc.

BibTeX

@misc{argushq_argushq_ai_company_prismatik_dentalcraft_inc_2026,
  title = {Regulatory Record: Prismatik Dentalcraft, Inc.},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/company/prismatik-dentalcraft-inc},
  note = {Accessed: August 4, 2026}
}

Source: FDA.gov (aggregated across Warning Letters, Recalls, Approvals, Form 483s) ↗