UFP TECHNOLOGIES, INC.

FDA Device Registration & Listing · Denver, CO, US · Registration 3009484708

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3009484708
FEI Number
3009484708
Entity Name
UFP TECHNOLOGIES, INC.
City/State/Country
Denver, CO, US
Establishment Address
707 Umatilla St, Denver, CO 80204, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
UFP Technologies, Inc. (Owner Number: 10052310)
Owner / Operator Contact Address
100 Hale St., Newburyport, MA 01950, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Biopsy foam pads

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IDZ Cassettes, Tissue Pathology Class 1 864.3010 2016-07-13

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

UFP Technologies, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3012456427 UFP TECHNOLOGIES, INC. Newburyport, MA, US
2020678 UFP Technologies, Inc. Compton, CA, US
1221541 CONTECH MEDICAL, INC. PROVIDENCE, RI, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009484708. Last updated year: 2026. Please use registration number 3009484708 when referencing this establishment in official correspondence.
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