Data / Medical devices / United States / Emsere, Inc.
Emsere, Inc.: FDA-registered device maker in Peachtree City, GA, United States, 49 510(k) clearances
Emsere, Inc. is registered with the FDA (registration 3010082909) in Peachtree City, GA, United States. It lists 30 device types. The FDA files 49 510(k) clearances under its listings, the newest dated December 5, 2025. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3010082909
- Address
- 627 Highway 74 South Suite 220, Peachtree City, GA, United States, 30269
- Owner or operator
- Emsere, Inc (10047331)
- Roles
- Repackager or relabeler
- First device listed
- August 11, 2014
- Registered through
- 2027
- Brand names listed
- 3-Liter Calibration Syringe 2030-2, B. BRAUN MEDICAL, INC., BBraun Medical Inc, BD EleVation Breast Biopsy System REF: EVDriver, BD Elevation Breast Biopsy Probe 10G x 10cm REF: EV10, 5/Case, Bp TRU BPM-200 Signs Monitor, CAESAREA MEDICAL ELECTRONICS LTD., COOL INCUBATOR 23 120V; COOL TOWER 23 120V; INCUBATOR 10 120V; INCUBATOR 10 Analog 120V; INCUBATOR 23 120V; INCUBATOR 56 120V; WATER BATH 6 120V and more
Devices it lists
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| December 5, 2025 | K252498 | Digital Color Doppler Ultrasound System (X11 Exp/X11 Elite/X11 Pro/X11 Plus/X11 Super/X11 Senior/X11/E11/E11 Pro/E11 Plus/E11 Elite/X11T/X11U/X11R/X11i/X11s/E11T/E11i/E11s/XR1/XR2/ XR3/ER1/ER2/ER3/X10 Exp/X10 Elite/X10 Pro/X10 Plus/X10 Super/X10 Senior/X10/X10T/X10U/ X10R/X10i/X10s/E10/E10 Pro/E10 Plus/E10T/E10i/E10s/SU11A EXP/SU11A PRO/SU11A AD/ SU11A CU/SU11B EXP/SU11B PRO/SU11B AD/SU11B CU/SU11C EXP/SU11C PRO/SU11C AD/ SU11C CU) | IYN | Substantially Equivalent | Sonoscape Medical Corp. | accessdata.fda.gov |
| April 17, 2025 | K243878 | CLARUS (700) | QER | Substantially Equivalent | Carl Zeiss Meditec, Inc. | accessdata.fda.gov |
| November 15, 2021 | K213436 | Clarius Ultrasound Scanner | IYN | Substantially Equivalent | Clarius Mobile Health Corp. | accessdata.fda.gov |
| March 31, 2021 | K210654 | EnCor Breast Biopsy Probe with Rinse Tube | KNW | Substantially Equivalent | Senorx, Inc. | accessdata.fda.gov |
| December 29, 2020 | K202456 | M5 Recorder | DSH | Substantially Equivalent | Global Instrumentation, LLC | accessdata.fda.gov |
| June 18, 2020 | K200297 | Microlife Upper Arm Automatic Digital Blood Pressure Monitor | DXN | Substantially Equivalent | Microlife Intellectual Property GmbH | accessdata.fda.gov |
| November 7, 2019 | K192948 | EleVation Breast Biopsy Driver, EleVation Breast Biopsy Probe - 10G, EleVation Breast Biopsy Probe - 14G | KNW | Substantially Equivalent | Bard Peripheral Vascular, Inc. | accessdata.fda.gov |
| September 25, 2019 | K190022 | SafeBreath Filter Mouthpiece | CAH | Substantially Equivalent | MD Diagnostics Limited | accessdata.fda.gov |
| August 29, 2019 | K192107 | Clarius Ultrasound Scanner | IYN | Substantially Equivalent | Clarius Mobile Health Corp. | accessdata.fda.gov |
| May 16, 2019 | K173895 | Tel-O-Graph | DXN | Substantially Equivalent | I.E.M. Industrielle Entwicklung and Medizintechnik | accessdata.fda.gov |
| February 15, 2019 | K183072 | EndoFLIP System | FFX | Substantially Equivalent | Crospon, Ltd. | accessdata.fda.gov |
| November 8, 2018 | K182030 | Faros Mobile | MLO | Substantially Equivalent | Bittium Biosignals , Ltd. | accessdata.fda.gov |
| November 22, 2017 | K170983 | NIOX VERO | MXA | Substantially Equivalent | Circassia AB | accessdata.fda.gov |
| January 5, 2017 | K161536 | EasyOne Air Spirometer | BZG | Substantially Equivalent | Ndd Medizintechnik AG | accessdata.fda.gov |
| June 18, 2015 | K142596 | Infusomat Space Volumetric Infusion Pump | FRN | Substantially Equivalent | B.Braun Medical, Inc. | accessdata.fda.gov |
| February 26, 2015 | K150233 | NIOX VERO Airway Inflammation Monitor | MXA | Substantially Equivalent | Aerocrine AB | accessdata.fda.gov |
| November 6, 2014 | K133898 | NIOX VERO AIRWAY INFLAMMATION MONITOR | MXA | Substantially Equivalent | Aerocrine AB | accessdata.fda.gov |
| October 4, 2012 | K122384 | MINISPIR | BZG | Substantially Equivalent | Mir Medical Intl. Research Srl | accessdata.fda.gov |
| August 2, 2012 | K122073 | ELI 280 ELECTROCARDIOGRAPH | DPS | Substantially Equivalent | Mortara Instrument, Inc. | accessdata.fda.gov |
| January 27, 2012 | K113185 | MODEL HBP-1300 | DXN | Substantially Equivalent | Omron Healthcare, Inc. | accessdata.fda.gov |
| December 16, 2011 | K110603 | HYPERTENSION MANAGEMENT SOFTWARE CLAIENT SERVER (HMS-CS) | DXN | Substantially Equivalent | I.E.M. GmbH | accessdata.fda.gov |
| November 21, 2011 | K103530 | SPIRODOC | BZG | Substantially Equivalent | Medical International Research USA, Inc. | accessdata.fda.gov |
| October 24, 2011 | K112177 | SOFIA ANALYZER AND INFLUENZA A+B FIA | PSZ | Substantially Equivalent | Quidel Corp. | accessdata.fda.gov |
| February 4, 2011 | K103732 | SPACELABS MODEL 90217A AMBULATORY BLOOD PRESSURE (ABP) MONITOR | DXN | Substantially Equivalent | Spacelabs Healthcare, Ltd. | accessdata.fda.gov |
| September 2, 2010 | K101034 | NIOX MINO MODEL 09-1000 | MXA | Substantially Equivalent | Aerocrine AB | accessdata.fda.gov |
| July 2, 2010 | K101403 | ELI 250 ELECTROCARDIOGRAPH | DPS | Substantially Equivalent | Mortara Instrument, Inc. | accessdata.fda.gov |
| June 18, 2010 | K101115 | ELI 150 ELECTROCARDIOGRAPH MODEL ELI 150 | DPS | Substantially Equivalent | Mortara Instrument, Inc. | accessdata.fda.gov |
| May 28, 2010 | K101275 | MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, WATCH BP OFFICE AFIB (TWIN200 AFS). | DXN | Substantially Equivalent | Microlife Intellectual Property GmbH | accessdata.fda.gov |
| April 16, 2010 | K100127 | ELI 230 ELECTROCARDIOGRAPH | DPS | Substantially Equivalent | Mortara Instrument, Inc. | accessdata.fda.gov |
| November 4, 2009 | K092313 | PERFUSOR SPACE INFUSION SYRINGE PUMP SYSTEM | MEA | Substantially Equivalent | B.Braun Medical, Inc. | accessdata.fda.gov |
| July 1, 2009 | K083689 | INFUSOMAT SPACE VOLUMETRIC INFUSION PUMP SYSTEM | FRN | Substantially Equivalent | B.Braun Medical, Inc. | accessdata.fda.gov |
| December 17, 2008 | K082766 | MODIFICATION TO MINISPIR, SPIROLAB III | BZG | Substantially Equivalent | Mir Medical Intl. Research Srl | accessdata.fda.gov |
| October 29, 2008 | K082357 | MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, MODELWATCHBP OFFICE (TWIN200). | DXN | Substantially Equivalent | Microlife Intellectual Property GmbH | accessdata.fda.gov |
| May 16, 2008 | K080954 | T34L SYRINGE DRIVER | FRN | Substantially Equivalent | Caesarea Medical Electronics , Ltd. | accessdata.fda.gov |
| May 2, 2007 | K070750 | 247 BP DEVICE | DXN | Substantially Equivalent | Suntech Medical, Inc. | accessdata.fda.gov |
| October 26, 2006 | K062700 | INFUSOMAT SPACE VOLUMETRIC INFUSION PUMP SYSTEM | FRN | Substantially Equivalent | B.Braun Medical, Inc. | accessdata.fda.gov |
| October 26, 2006 | K062699 | PERFUSOR SPACE INFUSION SYRINGE PUMP SYSTEM | FRN | Substantially Equivalent | B.Braun Medical, Inc. | accessdata.fda.gov |
| November 23, 2005 | K050800 | NIKI T34 AND BODYGUARD T34 SYRINGE DRIVERS | FRN | Substantially Equivalent | Caesarea Medical Electronics , Ltd. | accessdata.fda.gov |
| September 26, 2005 | K051730 | MATRIX HOLTER SYSTEM, MODEL M12 | MLO | Substantially Equivalent | Global Instrumentation, LLC | accessdata.fda.gov |
| March 11, 2005 | K042696 | BODYGUARD INFUSION PUMP SYSTEM | FRN | Substantially Equivalent | Caesarea Medical Electronics , Ltd. | accessdata.fda.gov |
| June 18, 2004 | K041313 | STABIL-O-GRAPH | DXN | Substantially Equivalent | I.E.M. GmbH | accessdata.fda.gov |
| February 11, 2004 | K032305 | OMRON INTELLISENSE DIGITAL BLOOD PRESSURE MONITOR, MODEL HEM-907XL | DXN | Substantially Equivalent | Omron Healthcare, Inc. | accessdata.fda.gov |
| October 22, 2002 | K023055 | BPTRU PORTABLE AUTOMATED NON-INVASIVE BLOOD PRESSURE MONITOR, MODEL BPM-200 | DXN | Substantially Equivalent | Vsm Medtech , Ltd. | accessdata.fda.gov |
| June 27, 2002 | K021373 | H12+HOLTER RECORDER | MWJ | Substantially Equivalent | Mortara Instrument, Inc. | accessdata.fda.gov |
| March 17, 1999 | K983945 | CORTEX DERMASCAN C ULTRASONIC SYSTEM | IYO | Substantially Equivalent | Cortex Technology Aps | accessdata.fda.gov |
| March 12, 1998 | K973403 | CARDIOSMART ST | LOS | Substantially Equivalent | Marquette Medical Systems, Inc. | accessdata.fda.gov |
| June 10, 1997 | K963717 | MILLEX - MP FILTER UNIT (SLMPO25SS/SLMPL25SS) | BSN | Substantially Equivalent | Millipore Corp. | accessdata.fda.gov |
| March 3, 1992 | K915436 | BLADDERSCAN BVI 2500 | IYO | Substantially Equivalent | Diagnostic Ultrasound Corp. | accessdata.fda.gov |
| November 6, 1991 | K913523 | AUTO. OSCILLOMETRIC DIGITAL BLOOD PRESS. MONITOR | DXN | Substantially Equivalent | Omron Healthcare, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of System, Measurement, Blood-Pressure, Non-Invasive
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- All makers of Pump, Infusion
- All makers of Set, Administration, Intravascular
- All makers of Pump, Infusion, Pca
Updated December 5, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.