Company ยท US
Trylon Corp.
FDA 510(k) clearances and medical device recalls filed under this name, 1995 to 2004. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Nov 22, 2004 | K033033 | VIZILITE-BLUE ORAL EXAM KIT Trylon Corp. | EAZ |
| Feb 22, 2002 | K011488 | SPIRABRUSH CX BIOPSY INSTRUMENT Trylon Corp. | HFB |
| Nov 27, 2001 | K012070 | ORALLITE COMPREHENSIVE EXAM TRAY Trylon Corp. | MPU |
| Mar 16, 2001 | K003995 | SPECULITE/ORALLITE Trylon Corp. | EAZ |
| Dec 12, 1997 | K963391 | SPECULITE Trylon Corp. | MPU |
| Mar 21, 1996 | K955790 | PAP PLUS SPECULOSCOPY COMPREHENSIVE PELVIC EXAM TRAY Trylon Corp. | HIC |
| Dec 8, 1995 | K953364 | SPECULITE Trylon Corp. | HET |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||