Panels › Obstetrics/Gynecology › Product code KXP · Class 2
Stent, Vaginal
Regulation 884.3900
0510(k)s in 12 months (4 all time)
0recalls in 12 months (0 all time)
0recalls that name a 510(k)
Top companies in KXP
| Company | 510(k)s | Recalls |
|---|---|---|
| Bioteque America, Inc. | 1 | 0 |
| Owen Mumford USA, Inc. | 1 | 0 |
| Pmt Corporation | 1 | 0 |
| Silimed, LLC | 1 | 0 |
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 30, 2020 | K202542 | Allura Vaginal Stent Pmt Corporation | KXP |
| Nov 25, 1998 | K983045 | AMIELLE Owen Mumford USA, Inc. | KXP |
| Aug 5, 1998 | K974479 | SILIMED VAGINAL STENT Silimed, LLC | KXP |
| Nov 8, 1995 | K920633 | PESSARY FLEXIBLE SILICONE NICHOLS Bioteque America, Inc. | KXP |
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