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 Pos-T-Vac with 12 510(k) clearances. The most recent is a 510(k) clearance dated Apr 4, 2002: SUPPORT SLEEVE.
| Apr 4, 2002 | SUPPORT SLEEVEK020258 · LKY | 510(k) clearances |
| Apr 4, 2002 | VT-1K020154 · LKY | 510(k) clearances |
| Nov 9, 2001 | BOSS-2000-2 VACUUM ERECTION DEVICEK012672 · LKY | 510(k) clearances |
| Nov 9, 2001 | BOSS 2000-3 VACUUM ERECTION DEVICEK012670 · LKY | 510(k) clearances |
| Nov 2, 1998 | POS-T-VAC (AVP-1000)K983245 · LKY | 510(k) clearances |
| Nov 2, 1998 | POS-T-VAC (IVP-600)K983246 · LKY | 510(k) clearances |
| Aug 28, 1998 | POS-T-VAC (REJOYN VACUUM ERECTION DEVICE)K981011 · LKY | 510(k) clearances |
| Aug 28, 1998 | REJOYN CONSTRICTION RING KIT, POS-T-VAC B-100 RING KIT, POS-T-VAC B-25 RING KIT AND POS-T-VAC B-10 RING KITK981180 · LKY | 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
