Data / Medical devices / United States / Axiom Medical, Inc.
Axiom Medical, Inc.: FDA-registered device maker in Torrance, CA, United States, 13 510(k) clearances
Axiom Medical, Inc. is registered with the FDA (registration 2020735) in Torrance, CA, United States. It lists 11 device types. The FDA files 13 510(k) clearances under its listings, the newest dated May 17, 2000. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2020735
- Address
- 19320 South Van Ness Ave., Torrance, CA, United States, 90501
- Owner or operator
- AXIOM MEDICAL, INC. (2020735)
- Roles
- Manufacturer
- First device listed
- March 30, 1978
- Registered through
- 2026
- Brand names listed
- AXIOM CLOSED WOUND, Atraum(TM), Axim(R) Atraum(TM) Mediastinal Silicone Drain, Axiom(R), Axiom(R) 3M Closed Wound Vacuum Drainage System, Axiom(R) Abdominal Dual-Sump, Axiom(R) Abdominal Filtered Dual-Sump, Axiom(R) Abdominal Uni-Sump and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Apparatus, Suction, Single Patient Use, Portable, Nonpowered | GCY | 1 | Manufacturer | accessdata.fda.gov |
| Bottle, Collection, Vacuum | KDQ | 2 | Manufacturer | accessdata.fda.gov |
| Catheter (Gastric, Colonic, Etc.), Irrigation And Aspiration | KDH | 2 | Manufacturer | accessdata.fda.gov |
| Catheter And Tip, Suction | JOL | 2 | Manufacturer | accessdata.fda.gov |
| Catheter, Conduction, Anesthetic | BSO | 2 | Manufacturer | accessdata.fda.gov |
| Catheter, Irrigation | GBX | 1 | Manufacturer | accessdata.fda.gov |
| Catheter, Percutaneous | DQY | 2 | Manufacturer | accessdata.fda.gov |
| Catheter, Ventricular, General & Plastic Surgery | GBS | 1 | Manufacturer | accessdata.fda.gov |
| Instrument, Surgical, Disposable | KDC | 1 | Manufacturer | accessdata.fda.gov |
| Tube, Double Lumen For Intestinal Decompression And/Or Intubation | FEG | 2 | Manufacturer | accessdata.fda.gov |
| Tubing, Noninvasive | GAZ | 2 | 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 |
|---|---|---|---|---|---|---|
| May 17, 2000 | K993592 | AXIOM MULTIPURPOSE WOUND DRAIN | BSO | Substantially Equivalent | Axiom Medical, Inc. | accessdata.fda.gov |
| January 22, 1998 | K971851 | INTERPLEURAL ANESTHESIA CATHETER | BSO | Substantially Equivalent | Axiom Medical, Inc. | accessdata.fda.gov |
| March 10, 1997 | K965146 | FLAT CLOSED WOUND DRAIN WITH TROCAR | GBX | Substantially Equivalent | Axiom Medical, Inc. | accessdata.fda.gov |
| February 17, 1989 | K883887 | AXIOM ATRAUM WOUND DRAINS | GBS | Substantially Equivalent | Axiom, Inc. | accessdata.fda.gov |
| August 29, 1986 | K863247 | AXIOM TROCAR THORACIC CATHETER | GBS | Substantially Equivalent | Axiom Medical, Inc. | accessdata.fda.gov |
| August 1, 1984 | K842084 | AXIOM FEMORAL VENUS CATHETER | DQY | Substantially Equivalent | Axiom Medical, Inc. | accessdata.fda.gov |
| June 5, 1984 | K841593 | AXIOM THORACIC CATHETERS | Substantially Equivalent | Axiom Medical, Inc. | accessdata.fda.gov | |
| March 15, 1982 | K820161 | AXIOM LIG-A-BOOTS | KDC | Substantially Equivalent | Axiom Medical, Inc. | accessdata.fda.gov |
| March 25, 1980 | K800015 | AXIOM VESSEL LOOPS | KDC | Substantially Equivalent | Axiom Medical, Inc. | accessdata.fda.gov |
| April 26, 1979 | K790654 | CLOSED WOUND VACUUM DRAINAGE SYSTEM | GCY | Substantially Equivalent | 3M Company | accessdata.fda.gov |
| December 4, 1978 | K781749 | TUBING, AXIOM SILICONE PENROSE | KDH | Substantially Equivalent | Axiom Medical, Inc. | accessdata.fda.gov |
| July 29, 1977 | K770983 | CATHETER THORACIC, AXIOM | JOL | Substantially Equivalent | Axiom Medical, Inc. | accessdata.fda.gov |
| July 19, 1977 | K771048 | CATHETERS, DRAINAGE | FEG | Substantially Equivalent | Axiom Medical, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Instrument, Surgical, Disposable
- All makers of Catheter And Tip, Suction
- All makers of Tubing, Noninvasive
- All makers of Catheter, Conduction, Anesthetic
- All makers of Apparatus, Suction, Single Patient Use, Portable, Nonpowered
- All makers of Catheter, Irrigation
Updated May 17, 2000. 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.