MOOSNI INTERNACIONAL SA DE CV

FDA Device Registration & Listing · HERMOSILLO Sonora, MX · Registration 3016219840

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
3016219840
FEI Number
3016219840
Entity Name
MOOSNI INTERNACIONAL SA DE CV
City/State/Country
HERMOSILLO Sonora, MX
Establishment Address
EUCALIPTOS 111, HERMOSILLO Sonora 83020, MX
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Ideavillage Products Corp. (Owner Number: 10031892)
Owner / Operator Contact Address
155 Route 46 West,, 4th FL., Wayne, NJ 07470, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

CopperFit Elite Ice Recovery Knee Copperfit Pro Knee Sleeve Copperfit Freedom Knee Sleeve Copperfit Elite Knee Sleeve Copperfit CBD Compression Knee Sleeve Copperfit ICE Compression Knee Sleeve Copperfit Work Gear Knee Sleeve Copperfit Advanced Compression Knee Stabilizer Copperfit Natural Motion Knee Brace CopperFit Air Series - Knee Copperfit X Knee Sleeve with Stabilizers Ultra Support Knee Stabilizer CopperFit Dual Action Knee Sleeve CopperFit Mobilizer Ankle Sleeve CopperFit Dual Action Ankle Sleeve CopperFit Arch Relief Support Wrap w/ Insert CopperFit Elite Ankle CopperFit Heel Relief L/XL CopperFit ICE Plantar Fascia Sleeve CopperFit Pro Ankle Sleeve Copper Fit Balance Insole Copper Fit Plantar Fascia Insole Copper Fit Heavy Duty Insole CF Arch Orthotic Insole Copper Fit Rapid Relief Elbow Copper Fit Rapid Relief Ankle Copper Fit Pro Back With Hot & Cold Gel Pack Copper Fit Rapid Relief Knee Copper Fit Rapid Relief Shoulder Copper Fit Rapid Relief Back Wrap Copper Fit Rapid Relief Plantar Fascia Copper Fit Rapid Relief Wrist

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ITQ Joint, Knee, External Brace Physical Medicine Class 1 890.3475 2018-02-21
ITW Joint, Ankle, External Brace Physical Medicine Class 1 890.3475 2018-02-21
IQI Orthosis, Limb Brace Physical Medicine Class 1 890.3475 2017-05-10
IME Pack, Hot Or Cold, Reusable Physical Medicine Class 1 890.5700 2018-03-15

Official Correspondent

No official correspondent registered.

US Agent Details

David Gulino Business: Idea Village Email: dgulino@ideavillage.com Phone: (973) 8268449

Related Public Records

Same Entity

Ideavillage Products Corp.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3013547648 DONGGUAN TIANYU SHOEFACTORY DONGGUAN Guangdong, CN
3020976343 Changshu Sanqiang Accessories Co., Ltd. Changshu Jiangsu, CN
2249769 IDEAVILLAGE PRODUCTS CORP. Wayne, NJ, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016219840. Last updated year: 2026. Please use registration number 3016219840 when referencing this establishment in official correspondence.
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