Cytophil, Inc

FDA Device Registration & Listing · East Troy, WI, US · Registration 3007225376

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
3007225376
FEI Number
3007225376
Entity Name
Cytophil, Inc
City/State/Country
East Troy, WI, US
Establishment Address
2485 Corporate Circle, Unit 2, East Troy, WI 53120, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Cytophil, Inc (Owner Number: 10025827)
Owner / Operator Contact Address
2485 Corporate Circle, Suite 2, East Troy, WI 53120, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MQV Filler, Bone Void, Calcium Compound Orthopedic Class 2 888.3045 2014-09-11
MQV Filler, Bone Void, Calcium Compound Orthopedic Class 2 888.3045 2014-05-20
MQV Filler, Bone Void, Calcium Compound Orthopedic Class 2 888.3045 2017-06-19
MQV Filler, Bone Void, Calcium Compound Orthopedic Class 2 888.3045 2019-03-22
MIX System, Vocal Cord Medialization Ear, Nose, Throat Class 2 874.3620 2015-04-16
MQV Filler, Bone Void, Calcium Compound Orthopedic Class 2 888.3045 2011-02-15

Official Correspondent

Greg Johnson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K180121 Cellumed Co., Ltd. Rafugen DBM 2018-04-11
K062691 Takiron Co., Ltd. COMPORUS 2008-04-15
K023703 Berkeley Advanced Biomaterials, Inc. BI-OSTETIC 2003-01-30
K173933 Xenco Medical, LLC Sorrento Bioglass Bone Graft Substitute 2018-09-13

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007225376. Last updated year: 2026. Please use registration number 3007225376 when referencing this establishment in official correspondence.
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