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Sign in to claim this brandKoven Technology, Inc.
United States·US-MF-000000948
Last updated September 17, 2026
About
Koven Technology provides vascular Dopplers & surgical Dopplers for peripheral arterial disease assessment and intraoperative vascular and cardiovascular procedures.
From the manufacturer's own website. Source
Information
- Country
- United States
- Address
- 625, 625 Maryville Centre Dr., St. Louis, United States
- Website
- www.koven.com
- —
- —
- [email protected]
- Phone
- +1 314 542 2101
- PRRC Contact
- Heather Bell
- EUDAMED SRN
- US-MF-000000948
- FDA FEI Number
- 1937397
- DUNS Number
- —
Catalogue (111)
Page 1 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Bt8m05s8a | BT8M05S8A | FDA UDI | Class II | Active |
| Pg-01 | PG-01 | FDA UDI | Class II | Active |
| F2m20s8a | F2M20S8A | FDA UDI | Class II | Unknown |
| T2m25n8a | T2M25N8A | FDA UDI | Class II | Active |
| NP Probe | NP20M12S8AF | FDA UDI | Class II | Active |
| VRP Probe | VRP-20 | FDA UDI | Class II | Active |
| Hd-307 | HD307--8 | FDA UDI | Class II | Active |
| Bt5m05s8a | BT5M05S8A | FDA UDI | Class II | Unknown |
| BiDop 3 | BiDop 3 | FDA UDI | Class II | Active |
| Pencil probe | PP8M05N5A | FDA UDI | Class II | Active |
| BiDop 7 | BiDop 7 | FDA UDI | Class II | Active |
| Doppler adaptor | AD8HD307 | FDA UDI | Class II | Active |
| NRP Probe | NRP-10H | FDA UDI | Class II | Active |
| Temp probe | TP-02 | FDA UDI | Class II | Unknown |
| BiDop 7 probe | ST10M5S8C | FDA UDI | Class II | Active |
| Adaptor | BDP08MS8 | FDA UDI | Class II | Active |
| Paus | 2.0 | FDA UDI | Class I | Active |
| Bf8m15s8a | BF8M15S8A | FDA UDI | Class II | Active |
| Bt10m5s8a | BT10M5S8A | FDA UDI | Class II | Active |
| Ct | CT-1 | FDA UDI | Class I | Active |
| Es102ex | ES102EX | FDA UDI | Class II | Active |
| NP Probe | NP20M12SF11 | FDA UDI | Class II | Active |
| Ct | CT-7 | FDA UDI | Class I | Active |
| BiDop 7 probe | PG-30 | FDA UDI | Class II | Active |
| Pv-21 | PV-21 | FDA UDI | Class II | Unknown |
| Adaptor | BDP10MS8 | FDA UDI | Class II | Active |
| Ct | CT-XT | FDA UDI | Class I | Active |
| Pgv-20 | PGV-20 | FDA UDI | Class II | Unknown |
| Temp Probe | TP-01 | FDA UDI | Class II | Active |
| Bt8m05s8c | BT8M05S8C | FDA UDI | Class II | Active |
| BiDop 7 probe | ST8M05S8A | FDA UDI | Class II | Active |
| FAST Sphyg | FAST Sphyg | FDA UDI | Class II | Active |
| VRP Probe | VRP-08 | FDA UDI | Class II | Active |
| Dvm 4500 | DVM 4500 | FDA UDI | Class II | Active |
| Lrp-08 | LRP-08 | FDA UDI | Class II | Active |
| Adaptor | DP20MS8 | FDA UDI | Class II | Active |
| Vdp-08a | VDP-08A | FDA UDI | Class II | Active |
| Pencil probe | BP10M5S8A | FDA UDI | Class II | Active |
| Smartdop XT6 | Smartdop XT6 | FDA UDI | Class II | Active |
| Bt10m5s8c | BT10M5S8C | FDA UDI | Class II | Active |
| Smartdop XT | Smartdop XT | FDA UDI | Class II | Active |
| Pencil probe | P10M5S8A | FDA UDI | Class II | Active |
| CRP Probe | CRP-20H1N | FDA UDI | Class II | Active |
| Smartdop 45 | Smartdop 45 | FDA UDI | Class II | Active |
| FDP Probe | FDP-20 | FDA UDI | Class II | Unknown |
| NP Probe | NP10M2S8AF | FDA UDI | Class II | Active |
| Bt8m05s8axt | BT8M05S8AXT | FDA UDI | Class II | Unknown |
| FDP Probe | FDP-8 | FDA UDI | Class II | Active |
| T5m05s8c | T5M05S8C | FDA UDI | Class II | Active |
| Pg-21 | PG-21 | FDA UDI | Class II | Active |
Related Companies
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Mar 4, 2026 | Z-1631-2026 | — | open, classified | Product labeling includes a fetal indication for use that is not cleared under its 510(k). |