Rog Sports Medicine, Inc.: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “Rog Sports Medicine, Inc.” (first 2011, latest 2011), across 1 product code in 1 review panel. Median 510(k) review time under this name: 63 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

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Top product codes

Product codeDeviceSubmissions510(k) clearances
MBIFastener, Fixation, Nondegradable, Soft Tissue55

Review panels

Most recent Rog Sports Medicine, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K113299ROG SUTURE ANCHORMBI2011-12-1537
K112991MODIFIED ROG SUTURE ANCHORMBI2011-12-0863
K111590ROG SUTURE ANCHOR, ROG KNOTLESS SUTURE ANCHORMBI2011-08-0862
K110230ROG KNOTLESS SUTURE ANCHORMBI2011-05-19113
K110229ROG SUTURE ANCHOR 5.5MM, 2.9MMMBI2011-05-18112

Recalls

openFDA lists no recalls under a recalling firm named Rog Sports Medicine, Inc..

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.

Frequently asked questions

How many FDA 510(k) clearances are listed under Rog Sports Medicine, Inc.?

FDA lists 5 510(k) clearances under the applicant name “Rog Sports Medicine, Inc.” (first 2011, latest 2011), across 1 product code 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 Rog Sports Medicine, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Rog Sports Medicine, Inc. is 63 days.

Which FDA product codes appear under Rog Sports Medicine, Inc.?

The most frequent FDA product codes under this applicant name are MBI (Fastener, Fixation, Nondegradable, Soft Tissue, 5).

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, with punctuation and legal suffixes removed; 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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