Data / Medical devices / United States / ContainMed, Inc.
ContainMed, Inc.: FDA-registered device maker in Indianapolis, IN, United States, 2 510(k) clearances
ContainMed, Inc. is registered with the FDA (registration 3007695749) in Indianapolis, IN, United States. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated December 12, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007695749
- Address
- 1841 Ludlow Ave, Indianapolis, IN, United States, 46201
- Owner or operator
- ContainMed, Inc (10029316)
- Roles
- Contract manufacturer, Manufacturer, Repackager or relabeler
- First device listed
- April 30, 2009
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Gauge, Depth | HTJ | 1 | Contract manufacturer | accessdata.fda.gov |
| Sterilization Wrap Containers, Trays, Cassettes & Other Accessories | KCT | 2 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Tray, Surgical, Instrument | FSM | 1 | Contract manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| December 12, 2023 | K233222 | Aygün Sterilization Container Systems | KCT | Substantially Equivalent | Aygun Surgical Instruments Co., Inc. | accessdata.fda.gov |
| September 9, 2008 | K071783 | VERSAPOD (TM) INSTRUMENT TRAYS | KCT | Substantially Equivalent | Containmed, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
- All makers of Tray, Surgical, Instrument
- All makers of Gauge, Depth
Updated December 12, 2023. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.