Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Integra LifeSciencesLabelled by claude-sonnet-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Camino Laboratories, Inc. with 18 510(k) clearances. The most recent is a 510(k) clearance dated Mar 30, 1995: CAMINO VENTRICULAR DRAINAGE SYSTEM.
| Mar 30, 1995 | CAMINO VENTRICULAR DRAINAGE SYSTEMK932769 · JXG | 510(k) clearances |
| Apr 15, 1993 | CAMINO VENTRICULAR ACCESS DEVICEK930222 · JXG | 510(k) clearances |
| Apr 15, 1993 | CAMINO VENTRICULAR TRANSDUCER ACCESSORYK930221 · GWM | 510(k) clearances |
| May 1, 1992 | CAMINO VENTRICULAR NEEDLEK920088 · HCD | 510(k) clearances |
| Jan 17, 1992 | VENTRICULAR PRESSURE MONITORING KIT, MODEL 110-4HMK914735 · GWM | 510(k) clearances |
| Sep 23, 1991 | CAMINO MODEL M420: MONIT INTER W/MEAN PRES DISPLAYK912833 · DSK | 510(k) clearances |
| Jul 14, 1989 | MODEL V420 DIRECT PRESSURE MONITOR & 427 WAVEFORMK893232 · DSK | 510(k) clearances |
| May 4, 1988 | VENTRICULAR BOLT PRESSURE MONITORING KIT #110-4HK881183 · GWM | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
