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 GlaxoSmithKlineLabelled 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 Safety Syringes, Inc. with 10 510(k) clearances. The most recent is a 510(k) clearance dated Mar 26, 2013: ULTRASAFE PLUS PASSIVE NEEDLE GUARD.
| Mar 26, 2013 | ULTRASAFE PLUS PASSIVE NEEDLE GUARDK123743 · MEG | 510(k) clearances |
| Sep 20, 2012 | ULTRASAFE PASSIVE NEEDLE GUARDK122558 · MEG | 510(k) clearances |
| Apr 28, 2006 | MODIFICATION TO: TAMPER EVIDENT ULTRASAFE PASSIVE DELIVERY SYSTEM, ULTRASAFE PASSIVE DELIVERY SYSTEM (X-SERIES)K060743 · MEG | 510(k) clearances |
| Oct 15, 2004 | TAMPER EVIDENT ULTRASAFE PASSIVE DELIVERY SYSTEMK042712 · MEG | 510(k) clearances |
| Dec 13, 2001 | ULTRASAFE DENTAL INJECTION SYSTEMK013801 · MEG | 510(k) clearances |
| May 29, 2001 | ULTRASAFE PASSIVE X-SERIES, NEEDLE GUARD SYRINGE, PISTON (ACCESSORY)K011369 · MEG | 510(k) clearances |
| Feb 26, 1998 | ULTRASAFE INJECTION SYSTEM MODEL C200 INJECTOR WITH NEEDLE GUARDK972877 · FMF | 510(k) clearances |
| Feb 26, 1998 | ULTRASAFE MODEL T200 INJECTORK972900 · FMF | 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
