Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007695749

FEI Number

3007695749

Entity Name

ContainMed, Inc.

City/State/Country

Indianapolis, IN, US

Establishment Address

1841 Ludlow Ave, Indianapolis, IN 46201, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

ContainMed, Inc (Owner Number: 10029316)

Owner / Operator Contact Address

1841 Ludlow Ave, Indianapolis, IN 46201, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K071783

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
HTJ	Gauge, Depth	Orthopedic	Class 1	888.4300	2023-03-13
FSM	Tray, Surgical, Instrument	General, Plastic Surgery	Class 1	878.4800	2017-03-14
KCT	Sterilization Wrap Containers, Trays, Cassettes & Other Accessories	General Hospital	Class 2	880.6850	2024-12-05
KCT	Sterilization Wrap Containers, Trays, Cassettes & Other Accessories	General Hospital	Class 2	880.6850	2009-04-30

Official Correspondent

Tyler Deal

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ContainMed, 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
K243425	Talladium España, SL	Guided DAS Surgical Kit	2025-07-22
K213209	K1 Medical, LLC	EZ-TRAX Zimmer G7 Acetabular System / Taperloc Complete Hip System Containment Device	2021-12-28
K012105	Symmetry Medical, Inc.	POLYVAC SURGICAL INSTRUMENT DELIVERY SYSTEM	2002-08-02
K243317	Infinitum Eta, Ltd.	NUVENTUS NV.C Surgical Cassette and Tray	2025-02-11
K112536	Covidien	SONICISION STERILIZATION TRAY	2012-04-19

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0027-2016	Zimmer, Inc.	1	Zimmer Universal Locking System, Titanium 3.5mm. Zimmer Implant and Instrument Cases are reusable, non-implantable devices designed to facilitate organization, identification, storage, transportation, cleaning, and sterilization processing of reusable instruments and certain unused implantable devices.

Similar Registrations

Registration Number	Establishment Name	Location
3005536892	Bioretec Ltd.	Tampere Pirkanmaa, FI
3019356409	INTELIVATION TECHNOLOGIES, LLC	Plymouth Meeting, PA, US
3004641308	ENZTEC LIMITED	CHRISTCHURCH Canterbury, NZ
3016112537	MAINSTREAM MEDICAL DEVICES	Austin, TX, US
1645151	CENTEX MACHINING, INC.	Round Rock, TX, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007695749. Last updated year: 2026. Please use registration number 3007695749 when referencing this establishment in official correspondence.