Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of TeleflexLabelled by claude-sonnet-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 Sheridan Catheter Corp. with 39 510(k) clearances. The most recent is a 510(k) clearance dated May 7, 1993: LAZER-TRACH TRACHEAL TUBE.
| May 7, 1993 | LAZER-TRACH TRACHEAL TUBEK922894 · BTR | 510(k) clearances |
| Mar 23, 1990 | LASER RESISTANT TRACHEAL TUBEK897046 · CBI | 510(k) clearances |
| May 5, 1989 | ACCESSORY TO CLINICAL ELECTRONIC THERMOMETERK890823 · FLL | 510(k) clearances |
| Feb 16, 1989 | CLINICAL ELECTRONIC THERMOMETERSK884765 · FLL | 510(k) clearances |
| Dec 5, 1988 | KIM NASO-INTESTINAL TUBEK882918 · KNT | 510(k) clearances |
| Aug 4, 1988 | CLINICAL ELECTRONIC THERMOMETERSK882127 · FLL | 510(k) clearances |
| Jul 13, 1988 | CLINICAL ELECTONIC THERMOMETERSK881368 · FLL | 510(k) clearances |
| Jun 16, 1988 | SHERIDAN ELECTROSURGERY PROTECTION FILTERK881293 · BZT | 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
