Superior Plastic Products Corp.: FDA filings under this applicant name

FDA lists 15 510(k) clearances under the applicant name “Superior Plastic Products Corp.” (first 1976, latest 1985), across 11 product codes in 4 review panels. Median 510(k) review time under this name: 76 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
KNTTubes, Gastrointestinal (And Accessories)44
JOLCatheter And Tip, Suction22
BSYCatheters, Suction, Tracheobronchial11
BTOTube, Tracheostomy (W/Wo Connector)11
FMHContainer, Specimen, Sterile11
FOZCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days11
FRNPump, Infusion11
GBXCatheter, Irrigation11
JCYCatheter, Infusion11
JOKScissors, Medical, Disposable11

Plus 1 more product codes.

Review panels

Most recent Superior Plastic Products Corp. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K851981NO. 5300-3 1/2 FRENCH UMBILICAL VESSEL CATH. ETC.FOZ1985-06-1842
K8439759 FRENCH 42LONG POLYURETHANE GRADUATED ENTERIC FEKNT1984-11-2040
K841945ENTERAL FEEDING BOTTLEKNT1984-07-2676
K841630ENTERAL NUTRITION PUMPFRN1984-06-0749
K841480INFECTION CONTROL VALVEBSY1984-04-2516
K840324SILICONE SUMP DRAIN 20 & 40 FRENCHJCY1984-04-2591
K840323SILICONE SUCTION & IRRIGATION DRAINGBX1984-04-2591
K833687DISPOS. ENTERIC FEEDING TUBES W/SAFE-TKNT1984-03-02123
K833947SUPERIOR ENTERNAL FEEDING SYSTEMKNT1984-02-0481
K8204603.5 & 5.5 OZ. SODIUM CHLORIDE SOLUTIONJOL1982-03-0817

5 earlier clearances. See the full list in Caduvo.

Recalls

openFDA lists no recalls under a recalling firm named Superior Plastic Products Corp..

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.

Related HCPCS codes

HCPCS Level II codes whose descriptors match the device names of the product codes filed under Superior Plastic Products Corp. (a text match, not an official crosswalk):

Other FDA applicant names starting with the same word

FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.

Frequently asked questions

How many FDA 510(k) clearances are listed under Superior Plastic Products Corp.?

FDA lists 15 510(k) clearances under the applicant name “Superior Plastic Products Corp.” (first 1976, latest 1985), across 11 product codes in 4 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 Superior Plastic Products Corp.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Superior Plastic Products Corp. is 76 days.

Which FDA product codes appear under Superior Plastic Products Corp.?

The most frequent FDA product codes under this applicant name are KNT (Tubes, Gastrointestinal (And Accessories), 4); JOL (Catheter And Tip, Suction, 2); BSY (Catheters, Suction, Tracheobronchial, 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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