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 13, 2026, FDA's public records list Std Mfg., Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Apr 10, 2003: CONTOURED ARTICULAR PROSTHESIS (CAP) HUMERAL HEAD RESURFACING SYSTEM.
| Date | Record | Source |
|---|---|---|
| Apr 10, 2003 | CONTOURED ARTICULAR PROSTHESIS (CAP) HUMERAL HEAD RESURFACING SYSTEMK023096 · HSD | 510(k) clearances |
| Aug 1, 2002 | CONTOURED ARTICULAR PROSTHESIS (CAP) FEMORAL HEAD RESURFACING SYSTEMK021549 · KXA | 510(k) clearances |
| Aug 23, 2001 | MODIFICATION TO VASCULAR CLOSURE DEVICEK012362 · GDW | 510(k) clearances |
| Dec 8, 2000 | VASCULAR CLOSURE DEVICEK003169 · GDW | 510(k) clearances |
| Mar 7, 2000 | SUCTION VASCULAR STAPLER AND IMPLANTABLE STAPLE SYSTEMK000608 · GDW | 510(k) clearances |
| Jun 1, 1993 | STD IRRIGATION PUMPK930427 · GCJ | 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
