Ahp Eos Buyer, Inc.: FDA filings under this applicant name
FDA lists 0 510(k) clearances under the applicant name “Ahp Eos Buyer, Inc.”, plus 4 PMA decisions, across 2 product codes 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 |
|---|---|---|---|
| LOE | Stimulator, Invasive Bone Growth | 2 | 0 |
| LOF | Stimulator, Bone Growth, Non-Invasive | 2 | 0 |
Review panels
- Orthopedic (4)
PMA and De Novo decisions
| Number | Pathway | Device | Decision date |
|---|---|---|---|
| P850035 | PMA | SpF® Implantable Spinal Fusion Stimulator | 1987-04-30 |
| P850022 | PMA | Biomet® OrthoPak® Non-invasive Bone Growth Stimulator System; Biomet® SpinalPak® Non-invasive Spine Fusion Stimulator Sy | 1986-02-18 |
| P790005 | PMA | OsteoGenTM Implantable Bone Growth Stimulators | 1980-01-25 |
| P790002 | PMA | Biomet(R) EBI BONE Healing System | 1979-11-06 |
Recalls
openFDA lists no recalls under a recalling firm named Ahp Eos Buyer, 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 Ahp Eos Buyer, Inc.?
FDA lists 0 510(k) clearances under the applicant name “Ahp Eos Buyer, Inc.”, plus 4 PMA decisions, across 2 product codes in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
Which FDA product codes appear under Ahp Eos Buyer, Inc.?
The most frequent FDA product codes under this applicant name are LOE (Stimulator, Invasive Bone Growth, 2); LOF (Stimulator, Bone Growth, Non-Invasive, 2).
Next steps
- See all 0 Ahp Eos Buyer, Inc. clearances with predicates and recalls
- Run predicate analysis for product code LOE, Ahp Eos Buyer, 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.