Data / Medical devices / United States / ARGENTUM MEDICAL, LLC dba Bravida Medical
ARGENTUM MEDICAL, LLC dba Bravida Medical: FDA-registered device maker in Geneva, IL, United States, 14 510(k) clearances
ARGENTUM MEDICAL, LLC dba Bravida Medical is registered with the FDA (registration 3003622638) in Geneva, IL, United States. It lists 8 device types. The FDA files 14 510(k) clearances under its listings, the newest dated July 31, 2024. Registered through 2027. FDA data exported November 3, 2026.
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- FDA registration number
- 3003622638
- Address
- 2571 Kaneville Ct, Geneva, IL, United States, 60134
- Owner or operator
- Argentum Medical, LLC (10045854)
- Roles
- Contract manufacturer, Manufacturer, Specification developer
- First device listed
- January 6, 2014
- Registered through
- 2027
- Brand names listed
- AnaSept Antimicrobial Skin & Wound Cleanser, AnaSept Antimicrobial Skin and Wound Gel, BioPlus+ Barrier Film, CathGrip, CathGrip Double Strip, XS, Oval, Single Strap, Medium LVAD Securement Device, Tube Securement Device, Faceplate Seals, Faceplate Strip, FreeDerm Adhesive remover, FreeDerm Bottles and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bandage, Elastic | FQM | 1 | Manufacturer | accessdata.fda.gov |
| Clamp, Penile | FHA | 1 | Manufacturer | accessdata.fda.gov |
| Device, Intravascular Catheter Securement | KMK | 1 | Manufacturer | accessdata.fda.gov |
| Device, Paste-On For Incontinence, Non-Sterile | NOA | 1 | Manufacturer | accessdata.fda.gov |
| Dressing, Wound, Drug | FRO | U | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Negative Pressure Wound Therapy Powered Suction Pump | OMP | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Solvent, Adhesive Tape | KOX | 1 | Specification developer | accessdata.fda.gov |
| Tape And Bandage, Adhesive | KGX | 1 | Specification developer | accessdata.fda.gov |
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 |
|---|---|---|---|---|---|---|
| July 31, 2024 | K241225 | Silverlon® Wound Contact, Burn Contact Dressing | FRO | Substantially Equivalent | Argentum Medical, LLC | accessdata.fda.gov |
| October 26, 2022 | K221218 | Silverlon Wound Contact, Burn Contact Dressings | FRO | Substantially Equivalent | Argentum Medical, Inc. | accessdata.fda.gov |
| July 18, 2019 | K190343 | Silverlon Wound Contact, Burn Contact Dressings | FRO | Substantially Equivalent | Argentum Medical, LLC | accessdata.fda.gov |
| January 14, 2019 | K180570 | Silverlon Island Wound Dressing, Silverlon Wound Pad Dressing (also known as Silverlon Burn Pad Dressing) | FRO | Substantially Equivalent | Argentum Medical, LLC | accessdata.fda.gov |
| April 30, 2015 | K150256 | SILVERLON BURN CONTACT DRESSINGS | FRO | Substantially Equivalent | Argentum Medical | accessdata.fda.gov |
| November 7, 2014 | K143001 | SILVERLON ISLAND WOUND DRESSING, SILVERLON WOUND PAD DRESSING | FRO | Substantially Equivalent | Argentum Medical | accessdata.fda.gov |
| September 12, 2014 | K141033 | SILVERLON ANTIMICROBIAL WOUND CONTACT NEGATIVE PRESSURE DRESSINGS, SILVERLON EASY AG ANTIMICROBIAL WOUND CONTACT NEGATIV | OMP | Substantially Equivalent | Argentum Medical, LLC | accessdata.fda.gov |
| August 28, 2014 | K141573 | SILVERLON ISLAND WOUND DRESSING | FRO | Substantially Equivalent | Argentum Medical | accessdata.fda.gov |
| May 28, 2008 | K073213 | THERABOND ANTIMICROBIAL BARRIER SYSTEMS | FRO | Substantially Equivalent | Choice Therapeutics | accessdata.fda.gov |
| April 23, 2008 | K073547 | ANASEPT ANTIMICROBIAL SKIN AND WOUND CLEANSERS; ANASEPT ANTIMICROBIAL SKIN AND WOUND GEL | FRO | Substantially Equivalent | Anacapa Technologies, Inc. | accessdata.fda.gov |
| November 21, 2006 | K062212 | SILVER SHIELD ANTIMICROBIAL SKIN AND WOUND GEL, MODEL 3015-S | FRO | Substantially Equivalent | Anacapa Technologies, Inc. | accessdata.fda.gov |
| October 6, 2006 | K053590 | SILVERLON CA (CALCIUM ALGINATE) | FRO | Substantially Equivalent | Argentum Medical, LLC | accessdata.fda.gov |
| January 17, 2003 | K023609 | SILVERLON ADHESIVE STRIP | FRO | Substantially Equivalent | Argentum International, LLC | accessdata.fda.gov |
| September 24, 1999 | K984210 | SILVERLON WOUND PACKING STRIPS | FRO | Substantially Equivalent | Argentum International, LLC | accessdata.fda.gov |
Compare with other makers
- All makers of Dressing, Wound, Drug
- All makers of Device, Paste-On For Incontinence, Non-Sterile
- All makers of Device, Intravascular Catheter Securement
- All makers of Tape And Bandage, Adhesive
- All makers of Solvent, Adhesive Tape
- All makers of Clamp, Penile
Updated July 31, 2024. 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.