Dispomed, Inc.: FDA filings under this applicant name

FDA lists 7 510(k) clearances under the applicant name “Dispomed, Inc.” (first 1989, latest 1989), across 5 product codes in 2 review panels. Median 510(k) review time under this name: 44 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
FXXMask, Surgical33
FYAGown, Surgical11
FYBGown, Patient11
KHRAbsorber, Saliva, Paper11
LYYLatex Patient Examination Glove11

Review panels

Most recent Dispomed, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K892748PATIENT EXAM GLOVES (MFG. AMMATEX)LYY1989-08-10121
K891054NON-STERILE GAUZE SPONGEKHR1989-05-0163
K891058DENTAL GOWNFYA1989-04-1244
K891056SURGICAL CONE MASKFXX1989-04-1244
K891053DENTAL BIBFYB1989-04-1244
K891052SPLASH GUARD GOGGLEFXX1989-04-1244
K891051SURGICAL FACE MASK-EAR LOOPFXX1989-04-1244

Recalls

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

FDA lists 7 510(k) clearances under the applicant name “Dispomed, Inc.” (first 1989, latest 1989), across 5 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 Dispomed, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Dispomed, Inc. is 44 days.

Which FDA product codes appear under Dispomed, Inc.?

The most frequent FDA product codes under this applicant name are FXX (Mask, Surgical, 3); FYA (Gown, Surgical, 1); FYB (Gown, Patient, 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, 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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