| Encor® | DRENCORMR | FDA UDI | Class II | Active |
| SenoMark® Breast Tissue Marker | SMEC10GSS | FDA UDI | Class II | Active |
| Encor® | FSENCOR01 | FDA UDI | Class II | Active |
| EnCor® | ECSTUS017G | FDA UDI | Class II | Unknown |
| Encor® | ECPMR017G | FDA UDI | Class II | Active |
| SenoMark® Breast Tissue Marker | SMTSU9G | FDA UDI | Class II | Active |
| Encor® | VACTUBEXT | FDA UDI | Class II | Active |
| Encor® | ECTT | FDA UDI | Class II | Active |
| SenoMark® Breast Tissue Marker | SMRSU12GT | FDA UDI | Class II | Active |
| Encor® | ECP0112GV | FDA UDI | Class II | Active |
| Encor® | ENCLRINSERT12G | FDA UDI | Class II | Active |
| Encor® | SCTUB3000 | FDA UDI | Class II | Active |
| EnCor | ENCFNGUIDE01 | FDA UDI | Class II | Active |
| Encor® | ECMRINTLOC7G | FDA UDI | Class II | Active |
| Encor® | ECP0110GV | FDA UDI | Class II | Active |
| Encor® | DRENCOR | FDA UDI | Class II | Active |
| Gel Mark Ultra™ Breast Tissue Marker | GMU11T | FDA UDI | Class II | Unknown |
| Gel Mark Ultra™ Breast Tissue Marker | MK2011 | FDA UDI | Class II | Unknown |
| Encor 7 Gauge | K051158 | FDA 510(k) | Class II | Active |
| EnCor Breast Biopsy Probe with Rinse Tube | K210654 | FDA 510(k) | Class II | Active |
| Contura Mlb Source Applicator For Brachytherapy | K081079 | FDA 510(k) | Class II | Active |
| Contura Cavity Maintenance Catheter | K092323 | FDA 510(k) | Class II | Active |
| Senorad Multi-Lumen Balloon Source Applicator For Branchytherapy | K071229 | FDA 510(k) | Class II | Active |
| Senorx Biopsy Device, Driver, Control Module, Including Accessories (power Cord, Connector Cords And Footswitch), Vacuums | K013641 | FDA 510(k) | Class II | Active |
| Contura Multi-Lumen Balloon Source Applicator For Brachytherapy, Models B001-45 And B011-45 | K080791 | FDA 510(k) | Class II | Active |
| Senorx Es-300 | K030473 | FDA 510(k) | Class II | Active |
| EnCor Enspire™Breast Biopsy System (E4115, E4230); EnCor™ Breast Biopsy Driver (DRENCOR); EnCor™ MRI Breast Biopsy Driver (DRENCORMR); EnCor™ Breast Biopsy Driver Probes (ECP017G, ECP017GV, ECP0110G, ECP0110GV, ECP0112G, ECP0112GV); EnCor™ MRI Breast Biopsy Probes (ECPMR017G, ECPMR0110G, ECPMR0110GBT) | K233220 | FDA 510(k) | Class II | Active |
| Senorx Biopsy Device Ii | K040842 | FDA 510(k) | Class II | Active |
| Easy Guide Electrosurgical Access Device | K012004 | FDA 510(k) | Class II | Active |
| Gel Mark Ultracor Biopsy Site Marker, Model: Gmuc-17ggp | K080698 | FDA 510(k) | Class II | Active |
| Senosonix Ultrasound Breast Biopsy System | K072541 | FDA 510(k) | Class II | Active |
| Gel Mark Biopsy Site Marker, Models Mkooo1, Mk0004, Mk0007 | K000060 | FDA 510(k) | Class II | Active |
| Anchor Guide Lesion Localization Device; Ancor Guide Holder; Rf Generator Cable | K012023 | FDA 510(k) | Class II | Active |
| Prostate Tissue Marker | K081170 | FDA 510(k) | Class II | Active |
| Gel Mark Iii Biopsy Site Marker | K031938 | FDA 510(k) | Class II | Active |
| Contura Lumen Marker | K082264 | FDA 510(k) | Class II | Active |
| Encor Breast Biopsy System | K093512 | FDA 510(k) | Class II | Active |
| Gel Mark Iv | K040706 | FDA 510(k) | Class II | Active |
| Starchmark Biopsy Site Marker, Model Stmkec-10gss, Stmkec-10gtr, Stmkmt-11gs | K081085 | FDA 510(k) | Class II | Active |
| Es-2000 Shape Select Electrosurgical Scalpel | K012799 | FDA 510(k) | Class II | Active |
| Biopsy Site Marker | K011402 | FDA 510(k) | Class II | Active |
| Senocor 360 Circumferential Vacuum Assisted Biopsy Device, 8 Gauge | K023923 | FDA 510(k) | Class II | Active |
| Starchmark Breast Tissue Marker; Starchmark Ultracor Breast Tissue Marker | K131654 | FDA 510(k) | Class II | Active |
| Gel Mark V | K050090 | FDA 510(k) | Class II | Active |
| Electrosurgical Generator System, Model Es 3000 | K052857 | FDA 510(k) | Class II | Active |
| EnCor MRI Introducer Set, EnCor Probe Introducer | K161805 | FDA 510(k) | Class II | Active |
| Single Step Biopsy Device, Single Step Surgical Handle, Single Step Driver, Single Step Holders | K021707 | FDA 510(k) | Class II | Active |
| Senorx Introducer | K042098 | FDA 510(k) | Class II | Active |