Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list PDG Product Design Group with 8 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Jun 27, 2017: Stellar LEAP.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jun 27, 2017 | Stellar LEAPK163432 · IOR | 510(k) clearances |
| Oct 16, 2014 | ELEVATIONK140023 · IOR | 510(k) clearances |
| Jun 12, 2012 | Fuze Manual Tilt Wheelchair. Fuze T50, Fuze T20 and Fuze T50 JrClass II · The hex bolt head might shear and cause the axle plate to detach from the lower frame of the wheelchair and could collap | Device recalls |
| Jan 17, 2007 | FUZE MECHANICAL WHEELCHAIR, MODELS T20 AND T50K063736 · IOR | 510(k) clearances |
| Jun 14, 2006 | ASTROTILT MANUAL WHEELCHAIRK061475 · IOR | 510(k) clearances |
| Mar 22, 1999 | THE STELLAR TILT, MANUALLY OPERATED WHEELCHAIRK990557 · IOR | 510(k) clearances |
| May 9, 1997 | ECLIPSE 400 MANUALLY OPERATED WHEELCAIRK971389 · IOR | 510(k) clearances |
| Feb 14, 1997 | BENTLEY MANUALLY OPERATED WHEELCHAIRK970311 · IOR | 510(k) clearances |
| May 29, 1996 | ECLIPSE 600 MANUALLY OPERATED WHEELCHAIRK961743 · IOR | 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
