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 Neward Enterprises, Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Aug 29, 1996: MITYVAC DIRECTIONAL VACUUM EXTRACTOR, DISPOSABLE.
| Aug 29, 1996 | MITYVAC DIRECTIONAL VACUUM EXTRACTOR, DISPOSABLEK960549 · HDB | 510(k) clearances |
| May 3, 1995 | MITYVAC SUPER M STYLE VACUM EXTRACTOR, DISPOSABLEK943938 · HDB | 510(k) clearances |
| May 4, 1994 | MITYVAC(R) OBSTETRIC VAC DELIV KIT W/UNIV VAC RELEASEK934011 · HDB | 510(k) clearances |
| Oct 8, 1993 | MITYVAC DISPOS-A-PLATE DISPOSABLE LEG PLATEK925572 · HGM | 510(k) clearances |
| Jun 22, 1992 | MITYVAC(R) SAFTISOFT OBSTETRICAL VACUUM DELIV KITK913324 · HDB | 510(k) clearances |
| Dec 10, 1991 | CR SPIRAL ELECTRODEK910815 · HGP | 510(k) clearances |
| Mar 31, 1989 | MITYVAC M STYLE VACUUM EXTRACTOR, DISPOSABLEK890307 · HDB | 510(k) clearances |
| Mar 12, 1984 | VENA * BRIDGEK840403 · | 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
