FIOMET VENTURES, INC

FDA Device Registration & Listing · Cincinnati, OH, US · Registration 3043668222

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
3043668222
FEI Number
3043668222
Entity Name
FIOMET VENTURES, INC
City/State/Country
Cincinnati, OH, US
Establishment Address
7737 Laurel Ave Ste 73, Cincinnati, OH 45243, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Fiomet Ventures, INC (Owner Number: 10095424)
Owner / Operator Contact Address
7737 LAUREL AVENUE, Suite 73, Cincinnati, OH 45243, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Le Squish Liquid-to-Foam Skin Pressure Protector — Horseshoe 5-Pack LS02-HS-5 Le Squish Liquid-to-Foam Skin Pressure Protector — Axillary 5-Pack LS01-AX-5 Le Squish Liquid-to-Foam Skin Pressure Protector — Axillary LS01-AX Le Squish Liquid-to-Foam Skin Pressure Protector — Horseshoe LS02-HS Le Squish Liquid-to-Foam Skin Pressure Protector — Pediatric Horseshoe LS03-HS-P Le Squish

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FMP Protector, Skin Pressure General Hospital Class 1 880.6450 2026-03-11

Official Correspondent

Scott Rapp

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Fiomet Ventures, INC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043668222. Last updated year: 2026. Please use registration number 3043668222 when referencing this establishment in official correspondence.
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