Changeflow GovPing Healthcare Acknowledgment Letter to Mom3nts Production
Routine Notice Added Final

Acknowledgment Letter to Mom3nts Production

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Summary

FDA's Center for Devices and Radiological Health (CDRH), Division of Manufacturers and Communication (DMB), issued an acknowledgment letter to Mom3nts Production. The letter confirms receipt of a submission filed under docket FDA-2025-V-3791. No documents are available for public viewing on Regulations.gov; the letter content is contained in an attachment.

What changed

FDA issued an acknowledgment letter to Mom3nts Production confirming receipt of a submission filed under docket FDA-2025-V-3791. The acknowledgment originates from CDRH's Division of Manufacturers and Communication, indicating this relates to a medical device matter. The actual letter content is contained in an attachment not publicly viewable on Regulations.gov.

Affected parties receiving FDA acknowledgment letters should monitor for any subsequent FDA correspondence, requests for additional information, or determinations related to their submission. This is routine administrative correspondence and does not itself impose compliance obligations.

What to do next

  1. Monitor Regulations.gov for any further correspondence regarding this submission

Archived snapshot

Apr 15, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

Content

There are no documents available to view or download

Attachments 1

Acknowledgment Letter from FDA DMB to Mom3nts Production

More Information
- Author(s) CDRH
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Last updated

Classification

Agency
FDA
Published
April 14th, 2025
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
FDA-2025-V-3791-0002
Docket
FDA-2025-V-3791

Who this affects

Applies to
Medical device makers
Industry sector
3345 Medical Device Manufacturing
Activity scope
Device submission filing Administrative correspondence
Geographic scope
United States US

Taxonomy

Primary area
Medical Devices
Operational domain
Regulatory Affairs
Compliance frameworks
GxP
Topics
Healthcare Administrative Law

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