Interpro Intl., Inc.: FDA filings under this applicant name
FDA lists 11 510(k) clearances under the applicant name “Interpro Intl., Inc.” (first 1987, latest 1989), across 7 product codes in 2 review panels. Median 510(k) review time under this name: 77 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
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| LYY | Latex Patient Examination Glove | 4 | 4 |
| EFQ | Gauze/Sponge, Internal | 2 | 2 |
| FXP | Cover, Shoe, Operating-Room | 1 | 1 |
| FYC | Gown, Isolation, Surgical | 1 | 1 |
| FYF | Cap, Surgical | 1 | 1 |
| KGO | Surgeon'S Gloves | 1 | 1 |
| LYZ | Vinyl Patient Examination Glove | 1 | 1 |
Review panels
Most recent Interpro Intl., Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K890968 | VINYL EXAMINATION GLOVES (MFG. SALZGITTER MOREX) | LYZ | 1989-07-31 | 154 |
| K891642 | PATIENT EXAMINATION GLOVES (LATEX) | LYY | 1989-07-14 | 119 |
| K890891 | LATEX EXAMINATION GLOVES (MFG. NINGBO MEDICAL) | LYY | 1989-07-14 | 142 |
| K891440 | PATIENT EXAMINATION GLOVES (LATEX) | LYY | 1989-05-31 | 77 |
| K891438 | PATIENT EXAMINATION GLOVES (LATEX) | LYY | 1989-05-31 | 77 |
| K881374 | SURGEONS GLOVES | KGO | 1988-08-05 | 126 |
| K874067 | GUAZE SPONGES | EFQ | 1987-12-14 | 70 |
| K874766 | INTERPRO INT'L, INC. ISOLATION GOWN | FYC | 1987-12-10 | 21 |
| K874066 | SURGICAL CAPS | FYF | 1987-11-04 | 30 |
| K874065 | LAPAROTOMY SPONGES | EFQ | 1987-11-04 | 30 |
1 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Interpro Intl., 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 Interpro Intl., Inc.?
FDA lists 11 510(k) clearances under the applicant name “Interpro Intl., Inc.” (first 1987, latest 1989), across 7 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 Interpro Intl., Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Interpro Intl., Inc. is 77 days.
Which FDA product codes appear under Interpro Intl., Inc.?
The most frequent FDA product codes under this applicant name are LYY (Latex Patient Examination Glove, 4); EFQ (Gauze/Sponge, Internal, 2); FXP (Cover, Shoe, Operating-Room, 1).
Next steps
- See all 11 Interpro Intl., Inc. clearances with predicates and recalls
- Run predicate analysis for product code LYY, Interpro Intl., Inc.'s most frequent
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.