Influx Pacific Sdn. Bhd.: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “Influx Pacific Sdn. Bhd.” (first 1989, latest 1998), across 3 product codes in 1 review panel. Median 510(k) review time under this name: 140 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
LYYLatex Patient Examination Glove22
LZAPolymer Patient Examination Glove22
KGOSurgeon'S Gloves11

Review panels

Most recent Influx Pacific Sdn. Bhd. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K980511NITRILE EXAMINATION GLOVES - POWDER FREELZA1998-03-1331
K970216NITRILE EXAMINATION GLOVES-PRE POWDEREDLZA1997-09-26253
K930407POWDER-FREE LATEX EXAMINATION GLOVESLYY1993-08-25211
K910895SURGICAL GLOVESKGO1991-07-22140
K891668PATIENT EXAMINATION GLOVES (LATEX)LYY1989-07-31133

Recalls

openFDA lists no recalls under a recalling firm named Influx Pacific Sdn. Bhd..

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 Influx Pacific Sdn. Bhd.?

FDA lists 5 510(k) clearances under the applicant name “Influx Pacific Sdn. Bhd.” (first 1989, latest 1998), across 3 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 Influx Pacific Sdn. Bhd.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Influx Pacific Sdn. Bhd. is 140 days.

Which FDA product codes appear under Influx Pacific Sdn. Bhd.?

The most frequent FDA product codes under this applicant name are LYY (Latex Patient Examination Glove, 2); LZA (Polymer Patient Examination Glove, 2); KGO (Surgeon'S Gloves, 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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