Orsonique, Inc.: FDA filings under this applicant name

FDA lists 6 510(k) clearances under the applicant name “Orsonique, Inc.” (first 1996, latest 1997), across 1 product code in 1 review panel. Median 510(k) review time under this name: 35 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
ESDHearing Aid, Air-Conduction, Prescription66

Review panels

Most recent Orsonique, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K972373OVATION HDPESD1997-07-2934
K963822OVATION AGC-3ESD1996-10-2835
K963821OVATION AGC-1ESD1996-10-2835
K963820OVATION LINEARESD1996-10-2835
K963819OVATION ASPESD1996-10-2835
K963818OVATION AGC-2ESD1996-10-2835

Recalls

openFDA lists no recalls under a recalling firm named Orsonique, 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 Orsonique, Inc.?

FDA lists 6 510(k) clearances under the applicant name “Orsonique, Inc.” (first 1996, latest 1997), 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 Orsonique, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Orsonique, Inc. is 35 days.

Which FDA product codes appear under Orsonique, Inc.?

The most frequent FDA product codes under this applicant name are ESD (Hearing Aid, Air-Conduction, Prescription, 6).

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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