John F. Greer Co., Inc.: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “John F. Greer Co., Inc.” (first 1986, latest 1987), across 3 product codes in 2 review panels. Median 510(k) review time under this name: 63 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 |
|---|---|---|---|
| EXB | Collector, Ostomy | 3 | 3 |
| KMK | Device, Intravascular Catheter Securement | 1 | 1 |
| KNX | Collector, Urine, (And Accessories) For Indwelling Catheter | 1 | 1 |
Review panels
Most recent John F. Greer Co., Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K870577 | E-Z LOOP | EXB | 1987-04-17 | 66 |
| K870531 | EZ TAC FILTER | EXB | 1987-04-10 | 63 |
| K864190 | E-Z HOLD - #4060 | KMK | 1987-01-14 | 79 |
| K864189 | ULTRA-GEL - #4083 | EXB | 1986-12-04 | 38 |
| K864188 | E-Z HOLD WITH ADHESIVE BASE.-#4065 | KNX | 1986-12-04 | 38 |
Recalls
openFDA lists no recalls under a recalling firm named John F. Greer Co., 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.
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.
- John O. Butler Co. (6 510(k)s)
- John Chatillon & Sons, Inc. (3 510(k)s)
- John Riccio (2 510(k)s)
- John Branch (1 510(k)s)
- John Caunt Scientific , Ltd. (1 510(k)s)
- John H. Harrison (1 510(k)s)
- John J. Navar, M.D. (1 510(k)s)
- John J Riccio (1 510(k)s)
- John M. Rayhack (1 510(k)s)
- John Mfg., Ltd. (1 510(k)s)
- John N. Haswell, M.D. (1 510(k)s)
- John W. King (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under John F. Greer Co., Inc.?
FDA lists 5 510(k) clearances under the applicant name “John F. Greer Co., Inc.” (first 1986, latest 1987), across 3 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 John F. Greer Co., Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name John F. Greer Co., Inc. is 63 days.
Which FDA product codes appear under John F. Greer Co., Inc.?
The most frequent FDA product codes under this applicant name are EXB (Collector, Ostomy, 3); KMK (Device, Intravascular Catheter Securement, 1); KNX (Collector, Urine, (And Accessories) For Indwelling Catheter, 1).
Next steps
- See all 5 John F. Greer Co., Inc. clearances with predicates and recalls
- Run predicate analysis for product code EXB, John F. Greer Co., 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.