Argentum International, LLC: FDA filings under this applicant name

FDA lists 8 510(k) clearances under the applicant name “Argentum International, LLC” (first 1998, latest 2007), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 236 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.

510(k) clearances per year

YearClearancesMedian review days
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Top product codes

Product codeDeviceSubmissions510(k) clearances
FRODressing, Wound, Drug77
KMFBandage, Liquid11

Review panels

Most recent Argentum International, LLC 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K984207SILVERLON DIRECT PRESSURE WOUND DRESSINGKMF2007-03-193037
K984205SILVERLON ADHESIVE STRIPFRO2007-03-193037
K984204SILVERLON DIRECT PRESSURE WOUND CLOSURE STRIPFRO2007-03-193037
K023612SILVERLON CONTACT WOUND DRESSINGFRO2003-01-2488
K023609SILVERLON ADHESIVE STRIPFRO2003-01-1781
K984210SILVERLON WOUND PACKING STRIPSFRO1999-09-24304
K984208SILVERLON ISLAND DRESSING, SILVERLON ISLAND PADFRO1999-02-2290
K981299SILVERLON CONTACT WOUND DRESSINGFRO1998-09-25169

Recalls

openFDA lists no recalls under a recalling firm named Argentum International, LLC.

Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.

Other FDA applicant names starting with the same word

FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.

Frequently asked questions

How many FDA 510(k) clearances are listed under Argentum International, LLC?

FDA lists 8 510(k) clearances under the applicant name “Argentum International, LLC” (first 1998, latest 2007), across 2 product codes in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.

How long has FDA taken to clear 510(k)s filed by Argentum International, LLC?

The median time from FDA receipt to decision across 510(k)s cleared under the name Argentum International, LLC is 236 days.

Which FDA product codes appear under Argentum International, LLC?

The most frequent FDA product codes under this applicant name are FRO (Dressing, Wound, Drug, 7); KMF (Bandage, Liquid, 1).

Next steps

Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name (spelling variants such as punctuation and legal suffixes combined); filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.

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