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 The Cooper CompaniesLabelled 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 Wallach Surgical Devices with 27 510(k) clearances. The most recent is a 510(k) clearance dated Jul 12, 2002: ENDOCERVICAL BLOCK NEEDLE.
| Jul 12, 2002 | ENDOCERVICAL BLOCK NEEDLEK021224 · HEE | 510(k) clearances |
| Jun 3, 2002 | WALLACH LOOP ELECTRODEK020711 · GEI | 510(k) clearances |
| Apr 11, 2000 | WALLACH QUANTUM 500 ELECTROSURGICAL GENERATORK000768 · EKZ | 510(k) clearances |
| Sep 29, 1999 | WALLACH'S ULTIMATE REUSABLE, PLASTIC VAGINAL SPECULUMK992736 · HIB | 510(k) clearances |
| Aug 12, 1999 | PMS 750 FINGERSWITCHK991669 · GEI | 510(k) clearances |
| May 20, 1999 | WALLACH QUANTUM 500 ELECTROSURGICAL GENERATOR (PROPOSED)K983840 · HGI | 510(k) clearances |
| Mar 1, 1999 | `THE INSEMINATOR' (PROPOSED)K984306 · MFD | 510(k) clearances |
| Feb 22, 1999 | WALLACH QUANTUM 500 ELECTROSURGICAL GENERATORK983208 · GEI | 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
