Ingredion Incorporated: FDA filings under this applicant name
FDA lists 0 510(k) clearances under the applicant name “Ingredion Incorporated”, plus 1 PMA decision, across 1 product code. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| KGP | 1 | 0 |
PMA and De Novo decisions
| Number | Pathway | Device | Decision date |
|---|---|---|---|
| N80535 | PMA | ABSORBO(R) DUSTING POWDER | 1973-03-02 |
Recalls
openFDA lists no recalls under a recalling firm named Ingredion Incorporated.
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.
SEC filings
Ingredion Inc (INGR): EDGAR filings, CIK 1046257. An SEC registrant with the same name, matched by name only.
Frequently asked questions
How many FDA 510(k) clearances are listed under Ingredion Incorporated?
FDA lists 0 510(k) clearances under the applicant name “Ingredion Incorporated”, plus 1 PMA decision, across 1 product code. Filings under other applicant names, such as subsidiaries, are not included.
Which FDA product codes appear under Ingredion Incorporated?
The most frequent FDA product codes under this applicant name are KGP (device, 1).
Next steps
- See all 0 Ingredion Incorporated clearances with predicates and recalls
- Run predicate analysis for product code KGP, Ingredion Incorporated'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 (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.