IPAX, INC.

FDA Device Registration & Listing · Englewood, CO, US · Registration 1720734

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
1720734
FEI Number
1720734
Entity Name
IPAX, INC.
City/State/Country
Englewood, CO, US
Establishment Address
2700 S Raritan St, Englewood, CO 80110, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
IPAX, INC. (Owner Number: 1720734)
Owner / Operator Contact Address
2700 South Raritan St., --, Englewood, CO 80110, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

G.I.D. 700 Tissue Canister TwoFer Transfer Needle Foundation DRS+ Duo FILLER, BONE VOID, CALCIUM COMPOUND Matrix 12M Esophageal Temperature Probe Foundation DRS Solo PLUS PAK Mayo Drape, Folded Synthecure

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MUU System, Suction, Lipoplasty General, Plastic Surgery Class 2 878.5040 2014-07-16
LHI Set, I.V. Fluid Transfer General Hospital Class 2 880.5440 2017-12-20
FRO Dressing, Wound, Drug Unknown Class U N/A 2026-03-06
MQV Filler, Bone Void, Calcium Compound Orthopedic Class 2 888.3045 2021-12-21
FLL Continuous Measurement Thermometer General Hospital Class 2 880.2910 2023-12-28
KGN Wound Dressing With Animal-Derived Material(S) Unknown Class U N/A 2026-03-06
BYX Tubing, Pressure And Accessories Anesthesiology Class 1 868.5860 1992-06-17
MQV Filler, Bone Void, Calcium Compound Orthopedic Class 2 888.3045 2025-07-08

Official Correspondent

Jeffery Baldwin

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

IPAX, 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
K243985 Icu Medical, Inc. Rio™ Drug Reconstitution Transfer Device 2025-01-22
K222718 Hangzhou Qiantang Longyue Biotechnology Co., Ltd. Vial Adapter 2023-03-10
K150256 Argentum Medical SILVERLON BURN CONTACT DRESSINGS 2015-04-30
K180121 Cellumed Co., Ltd. Rafugen DBM 2018-04-11
K062691 Takiron Co., Ltd. COMPORUS 2008-04-15

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0007-2017 Baxter Corporation Englewood 2
0.2 Micron Filter, 50 mm Product Usage: The 0.2 Micron Filter is a bacteria and particulate filter for aqueous solutions. It attaches to a standard Baxter Pharmacy Pump Tube Set.
Z-0003-06 B. Braun Medical, Inc. U
D-Stat Dry Hemostatic Bandage. The product is an adhesive bandage.
Z-0038-2025 3M Company Health Care Business 3m Center U
3M Tegaderm CHG, Chlorhexidine Gluconate I.V. Securement Dressing, REF 1658R

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1937141 THE METRIX COMPANY DUBUQUE, IA, US
3006798004 THIEBAUD SAS Paris Ile-de-France, FR
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1720734. Last updated year: 2026. Please use registration number 1720734 when referencing this establishment in official correspondence.
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