Medical device makerLabelled by claude-haiku-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 Inviro Medical Devices, Inc. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Aug 20, 2010: INVIROSTRIPE LUER LOCK SYRINGES (1, 3, 10, 20, 30 AND 60 ML).
| Aug 20, 2010 | INVIROSTRIPE LUER LOCK SYRINGES (1, 3, 10, 20, 30 AND 60 ML)K101359 · FMF | 510(k) clearances |
| Sep 4, 2009 | 1 ML FIXED NEEDLE, 3 ML LUER LOCK, 5 ML LUER LOCK, 10 ML LUER LOCK, 20 ML LUERL LOCK SAFETY SYRINGESK092430 · MEG | 510(k) clearances |
| Sep 4, 2009 | INVIROSNAP 50 AND 100 UNIT INSULIN SAFETY SYRINGESK092413 · MEG | 510(k) clearances |
| May 15, 2009 | INVIROBLUNT CANNULA WITH AND WITHOUT EZ WINGS, MODELS 120522 AND 120022K083851 · LHI | 510(k) clearances |
| Oct 22, 2008 | INVIROSTRIPE 3ML, 5ML, 10ML LUER LOCK SYRINGESK081436 · FMF | 510(k) clearances |
| Feb 12, 2008 | INVIROLINK AND INVIRO TIP BLUNT CANNULAS, MODEL 130001, 130501, 140001, 140002, 140003K071307 · FMI | 510(k) clearances |
| Apr 23, 2007 | INVIROSNAP SAFETY SYRINGE, MODELS 120006, 120007, 120008, 100080, 130022, 130023 AND 130024K070203 · MEG | 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
