Bayer Pharma AG: FDA filings under this applicant name
FDA lists 0 510(k) clearances under the applicant name “Bayer Pharma AG”, plus 1 PMA decision, across 1 product code in 1 review panel. 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 |
|---|---|---|---|
| HHS | Transcervical Contraceptive Tubal Occlusion Device | 1 | 0 |
Review panels
PMA and De Novo decisions
| Number | Pathway | Device | Decision date |
|---|---|---|---|
| P020014 | PMA | ESSURE SYSTEM | 2002-11-04 |
Recalls
openFDA lists no recalls under a recalling firm named Bayer Pharma AG.
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.
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.
- Bayer Corp. (96 510(k)s)
- Bayer Healthcare, LLC (55 510(k)s)
- Bayer Diagnostics Corp. (32 510(k)s)
- Bayer Medical Care, Inc. (10 510(k)s)
- Bayer Corp., Agfa Div. (3 510(k)s)
- Bayer Healthcare, Diagnostics Division (2 510(k)s)
- Bayer Group Diagnostics (2 510(k)s)
- Bayer U.S., LLC (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Bayer Pharma AG?
FDA lists 0 510(k) clearances under the applicant name “Bayer Pharma AG”, plus 1 PMA decision, across 1 product code in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
Which FDA product codes appear under Bayer Pharma AG?
The most frequent FDA product codes under this applicant name are HHS (Transcervical Contraceptive Tubal Occlusion Device, 1).
Next steps
- See all 0 Bayer Pharma AG clearances with predicates and recalls
- Run predicate analysis for product code HHS, Bayer Pharma AG'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.