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. Jamner Surgical Instruments, Inc. with 11 510(k) clearances. The most recent is a 510(k) clearance dated Nov 21, 2008: JARIT HULKA UTERINE TENACULUM FORCEPS.
| Nov 21, 2008 | JARIT HULKA UTERINE TENACULUM FORCEPSK082349 · HDC | 510(k) clearances |
| Feb 2, 1995 | JARIT RECOMMENDED SINUS INSTRUMENTSK944670 · EOB | 510(k) clearances |
| Nov 2, 1994 | JARIT ENDOSCOPES, MODELS 600-600; 600-630; 600-650; AND 600-680K944870 · GCJ | 510(k) clearances |
| May 16, 1994 | JARIT RECOMMENDED SINUS INSTRUMENTSK941565 · EOB | 510(k) clearances |
| Apr 21, 1994 | JARIT SURGICAL INSTRUMENTSK932456 · KNF | 510(k) clearances |
| Feb 23, 1994 | JARIT SURGICAL INSTRUMENTS: CATALOG 615-330, 615-331, 615-334, 615-335, 615-338, 615-339K933728 · GEI | 510(k) clearances |
| Nov 10, 1993 | JARIT SURGICAL INSTRUMENTSK931928 · GCJ | 510(k) clearances |
| Oct 5, 1993 | JARIT SURGICAL INSTRUMENTSK931959 · GEI | 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
