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 Panpac Medical Corporation with 12 510(k) clearances. The most recent is a 510(k) clearance dated Oct 31, 2018: Panpac Flexi Shelf Pessary.
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.
| Oct 31, 2018 | Panpac Flexi Shelf PessaryK173351 · HHW | 510(k) clearances |
| Jan 13, 2017 | PANPAC DISPOSABLE VACUUM CURETTESK161106 · HGH | 510(k) clearances |
| Jul 14, 2016 | Panpac Disposable Pessary Fitting SetK153422 · HHW | 510(k) clearances |
| Jun 4, 2014 | PANPAC INFLATABLE DOCUT PESSARYK132670 · HHW | 510(k) clearances |
| Jan 10, 2014 | PANPAC WORD/BARTHOLIN CATHETERK130087 · KNA | 510(k) clearances |
| Aug 8, 2013 | PANPAC VAGINAL DILATORSK130273 · HDX | 510(k) clearances |
| Dec 15, 2011 | BELLOTA SONOHYSTEROGRAPHY CATHETER WITH CERVICAL CONE, BELLOTA SONOHYSTEROGRAPHY CATHETER WITHOUT CERVICAL CONEK102898 · LKF | 510(k) clearances |
| Jul 26, 2010 | THE PANPAC SUCTION CURETTEK092982 · HHK | 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