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 Portlyn Corp. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Jun 17, 1997: DYNABITE HOT GI BIOPSY FORCEPS.
| Jun 17, 1997 | DYNABITE HOT GI BIOPSY FORCEPSK970083 · KGE | 510(k) clearances |
| Jul 27, 1995 | DYNABITE CARDIOVASCULAR BIOPSY FORCEPSK951447 · DWZ | 510(k) clearances |
| Jun 1, 1995 | DYNABITE UROLOGICAL FORCEPSK952391 · FCL | 510(k) clearances |
| Nov 15, 1994 | DYNABITE LAPAROSCOPIC FORCEPSK944245 · HET | 510(k) clearances |
| Mar 22, 1994 | DYNABITE HYSTEROSCOPIC FORCEPSK934506 · HET | 510(k) clearances |
| Jun 29, 1990 | BIOPSY FORCEPSK901300 · DWZ | 510(k) clearances |
| Apr 16, 1990 | BIOPSY FORCEP (NON-ELECTRIC)K896147 · FCL | 510(k) clearances |
| Mar 9, 1990 | BIOPSY FORCEPS, (NON-RIGID)K896146 · EOQ | 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
