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 Penn Medical Devices with 8 510(k) clearances. The most recent is a 510(k) clearance dated Oct 20, 1987: RORERTAZZI NASOPHARYNGEAL AIRWAY.
| Oct 20, 1987 | RORERTAZZI NASOPHARYNGEAL AIRWAYK873949 · BTQ | 510(k) clearances |
| Oct 14, 1987 | DEVINE (SUPRAPUBIC SOUND AND GUIDE)K873177 · KOE | 510(k) clearances |
| Oct 14, 1987 | HUFFMAN BIOPSY UNITK873176 · FCL | 510(k) clearances |
| Sep 30, 1987 | URETERAL BULB DILATORSK873178 · EZN | 510(k) clearances |
| Jun 10, 1987 | URETERAL STENTK871667 · FAD | 510(k) clearances |
| May 11, 1987 | GASTROINTESTINAL TUBEK870508 · KNT | 510(k) clearances |
| Oct 24, 1986 | PENN 3-RING HANDLEK862729 · FFL | 510(k) clearances |
| Sep 11, 1986 | PENN & OLYMPUS URETEROSCOPY GUIDE SHEATH & DILATORK862107 · ODC | 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
