Horizon Medical Products, Inc. FDA Record
- No warning letters matched by name
Horizon Medical Products, Inc. has 0 FDA recalls, 0 inspections, 16 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Horizon Medical Products, Inc." is on file.
- Latest 510(k)
- Nov 18, 2003
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 16 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 0 | Nov 14, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
Reviewing Horizon Medical Products, Inc. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.
Or check Horizon Medical Products, Inc. yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.
Recent 510(k) clearances
| K-Number | Device | Date |
|---|---|---|
| K033473 | MODIFICATION TO VORTEX MP VASCULAR ACCESS PORT | Nov 18, 2003 |
| K032754 | VORTEX MP | Sep 12, 2003 |
| K032557 | TRIUMPH VTX WITH LIFEVALVE CATHETER | Sep 9, 2003 |
| K031718 | LIFEVALVE CENTRAL VENOUS CATHTER | Jul 2, 2003 |
| K022905 | LIFEJET F16 HEMODIALYSIS/APHERESIS CHRONIC CATHETER | Dec 13, 2002 |
| K013871 | LIFEGUARD SAFETY INFUSION SET | Mar 29, 2002 |
| K011916 | SUPER C HEMODIALYSIS/APHERESIS CHRONIC CATHETER, MODEL DC-36 SERIES, DC-40 SERIES, DC-45 SERIES | Oct 31, 2001 |
| K010767 | LIFEPORT VTX ACCESS SYSTEM,MODEL VTX 7000 SERIES | Apr 10, 2001 |
| K010189 | VORTEX ACCESS SYSTEM | Feb 12, 2001 |
| K994196 | HORIZON MEDICAL PRODUCTS MICROPORT 2 PERIPHERAL ACCESS PORT SYSTEM | Feb 10, 2000 |
| K951814 | TRIUMPH-1 PORT | Aug 29, 1995 |
| K934504 | HMP DUAL TITANIUM PORT | Feb 25, 1994 |
| K934640 | HMP DUAL POLYSULFONE PORT | Feb 25, 1994 |
| K933986 | HMP POLYSULFONE PORT | Feb 25, 1994 |
| K934573 | HMP TITANIUM LOW PROFILE PORT | Feb 25, 1994 |
| K933990 | HMP TITANIUM PORT | Feb 25, 1994 |
Horizon Medical Products, Inc. and the FDA: common questions
Has Horizon Medical Products, Inc. received an FDA warning letter?
No FDA warning letter addressed to the name "Horizon Medical Products, Inc." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.
Has Horizon Medical Products, Inc. received an FDA Form 483?
FDA has not published a Form 483 for "Horizon Medical Products, Inc." in its reading room. FDA publishes some Form 483s, not all of them.
Need more than this page shows? Ask about Horizon Medical Products, Inc. in Claude or ChatGPT and get every site's inspections, Form 483s, warning letters and import alerts, with a link to the FDA source for each record. The API key is free: no card.