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Sign in to claim this brandSumma Therapeutics
US
Last updated May 23, 2026
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Catalogue (103)
Page 2 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Finesse BTK Multicath | FS400601002 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS252251502 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS250400652 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS400201502 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS200200652 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS201001002 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS300200652 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS350400652 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS351000652 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS252250652 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS400600652 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS250601502 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS251000652 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS401001002 | FDA UDI | Class II | Active |
| Finesse Injectable PTA Balloon Dilatation Catheter OTW 014 | FS301001508 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS350401502 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS200400652 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS200601002 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS301001502 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS350601502 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS250601002 | FDA UDI | Class II | Active |
| Finesse Injectable PTA Balloon Dilatation Catheter OTW 014 | FS200201508 | FDA UDI | Class II | Active |
| Finesse Injectable PTA Balloon Dilatation Catheter OTW 014 | FS250401508 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS350201002 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS400401502 | FDA UDI | Class II | Active |
| Finesse Injectable PTA Balloon Dilatation Catheter OTW 014 | FS251001508 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS301000652 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS350601002 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS302251502 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS252251002 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS352250652 | FDA UDI | Class II | Active |
| Finesse Injectable PTA Balloon Dilatation Catheter OTW 014 | FS401001508 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS351001502 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS200600652 | FDA UDI | Class II | Active |
| Finesse Injectable PTA Balloon Dilatation Catheter OTW 014 | FS302251508 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS250600652 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS300401502 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS250201002 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS350200652 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS251001002 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS300601002 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS400400652 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS251001502 | FDA UDI | Class II | Active |
| Finesse Injectable PTA Balloon Dilatation Catheter OTW 014 | FS252251508 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS201001502 | FDA UDI | Class II | Active |
| Finesse Injectable PTA Balloon Dilatation Catheter OTW 014 | FS200601508 | FDA UDI | Class II | Active |
| Finesse Injectable PTA Balloon Dilatation Catheter OTW 014 | FS400201508 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS250201502 | FDA UDI | Class II | Active |
| Finesse BTK Multicath | FS402251002 | FDA UDI | Class II | Active |
| Finesse Injectable PTA Balloon Dilatation Catheter OTW 014 | FS300201508 | FDA UDI | Class II | Active |
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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 |
|---|---|---|---|---|
| Jul 21, 2025 | Z-1704-2026 | — | open, classified | Potential for the balloon in the device to not meet burst specifications. |