O.R. Solutions, Inc.: FDA filings under this applicant name

FDA lists 7 510(k) clearances under the applicant name “O.R. Solutions, Inc.” (first 1995, latest 2005), across 4 product codes in 2 review panels. Median 510(k) review time under this name: 51 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
LHCWarmer, Irrigation Solution44
KKXDrape, Surgical, Antimicrobial11
LRJDisinfectant, Medical Devices11
OCTAnti Fog Solution And Accessories, Endoscopy11

Review panels

Most recent O.R. Solutions, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K051979ORS MODEL 6000 ENDOSCOPE HOLDEROCT2005-08-3040
K0232831075LD HUSH-SLUSHLHC2002-11-1343
K023282ORS-3000LDLHC2002-11-1343
K021288ORS-1000LDLHC2002-06-2765
K021289WARMER 2000LDLHC2002-06-2664
K960836DMS-9000LRJ1996-09-12196
K953654ORS-111KKX1995-09-2251

Recalls

openFDA lists no recalls under a recalling firm named O.R. Solutions, 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 O.R. Solutions, Inc.?

FDA lists 7 510(k) clearances under the applicant name “O.R. Solutions, Inc.” (first 1995, latest 2005), across 4 product codes in 2 review panels. Filings under other applicant names, such as subsidiaries, are not included.

How long has FDA taken to clear 510(k)s filed by O.R. Solutions, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name O.R. Solutions, Inc. is 51 days.

Which FDA product codes appear under O.R. Solutions, Inc.?

The most frequent FDA product codes under this applicant name are LHC (Warmer, Irrigation Solution, 4); KKX (Drape, Surgical, Antimicrobial, 1); LRJ (Disinfectant, Medical Devices, 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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