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 J. Sklar Manufacturing with 18 510(k) clearances. The most recent is a 510(k) clearance dated Oct 31, 1984: JACOBS HIGH VACUUM SUCTION UNIT 05-2570.
| Oct 31, 1984 | JACOBS HIGH VACUUM SUCTION UNIT 05-2570K843693 · BTA | 510(k) clearances |
| Jul 3, 1984 | TISCHLER CERVICAL BIOPSY PUNCH FORCEPSK842112 · HFB | 510(k) clearances |
| Jun 19, 1984 | KOGAN ENDOSPECULUM 9-1/2K842111 · HTZ | 510(k) clearances |
| Sep 14, 1982 | SCISSORS, VARIOUSK822448 · FZT | 510(k) clearances |
| Jan 12, 1981 | KEVORKIAN-YOUNGE BIOPSY PUNCH, #90-6610K802457 · HFB | 510(k) clearances |
| Jan 12, 1981 | KEVORKIAN-YOUNGE BIOPSY CURETTE #90-6611K802458 · HFB | 510(k) clearances |
| Jul 28, 1980 | MAGILL CATHETER INTRO. FORCEPSK801273 · KOA | 510(k) clearances |
| Apr 8, 1980 | RUDD-CLINIC HEMORRHOIDAL FORCEPSK800441 · KOA | 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
