RESOLVE DESIGNS LLC

FDA Device Registration & Listing · Springville, UT, US · Registration 3013083631

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
3013083631
FEI Number
3013083631
Entity Name
RESOLVE DESIGNS LLC
City/State/Country
Springville, UT, US
Establishment Address
157 E 300 S, Springville, UT 84663, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Resolve Designs (Owner Number: 10052954)
Owner / Operator Contact Address
157 E 300 S, Springville, UT 84663, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

RxCrush Pill Pouch with Locking ENFit RxCrush Pediatric, Sealed, Tear Off Pill Pouch RxCrush Pediatric Pill Pouch with Locking ENFit Female ENFit® Pill Pouch Cap - Push-on Female ENFit® Pill Pouch Cap - Screw-on RX Crush Pill Crusher

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KYX Dispenser, Liquid Medication General Hospital Class 1 880.6430 2016-10-19
OHY Pill Crusher/Cutter General Hospital Class 1 880.6430 2016-10-19

Official Correspondent

Aaron Collett

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Resolve Designs
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013083631. Last updated year: 2026. Please use registration number 3013083631 when referencing this establishment in official correspondence.
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