Moss Medical Products: FDA filings under this applicant name
FDA lists 8 510(k) clearances under the applicant name “Moss Medical Products” (first 1991, latest 2005), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 143 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 |
|---|---|---|---|
| KNT | Tubes, Gastrointestinal (And Accessories) | 7 | 7 |
| FPD | Tube, Feeding | 1 | 1 |
Review panels
Most recent Moss Medical Products 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K051206 | Y2K2 ENTERNAL TUBE FLUID FILTER | KNT | 2005-11-02 | 175 |
| K030413 | Y2K2 ENTERNAL FEEDING MANAGER | KNT | 2004-05-11 | 459 |
| K031492 | MOSSMED DUAL INTERMITTENT ASPIRATOR | KNT | 2004-02-05 | 269 |
| K913701 | MOSS - ANCHOR SET | FPD | 1992-02-14 | 179 |
| K910910 | MOSS- ANCHOR SET | KNT | 1991-06-24 | 111 |
| K910912 | MOSS NASAL TUBE MARK IV | KNT | 1991-05-28 | 84 |
| K910911 | MOSS P.E.G. TRAY | KNT | 1991-05-03 | 59 |
| K910913 | MOSS GASTROSTOMY TUBE | KNT | 1991-04-19 | 45 |
Recalls
openFDA lists no recalls under a recalling firm named Moss Medical Products.
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.
- Moss Tubes, Inc. (5 510(k)s)
- Moss Point Glove Co. (1 510(k)s)
- Moss Rehabilation Hospital (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Moss Medical Products?
FDA lists 8 510(k) clearances under the applicant name “Moss Medical Products” (first 1991, latest 2005), across 2 product codes in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Moss Medical Products?
The median time from FDA receipt to decision across 510(k)s cleared under the name Moss Medical Products is 143 days.
Which FDA product codes appear under Moss Medical Products?
The most frequent FDA product codes under this applicant name are KNT (Tubes, Gastrointestinal (And Accessories), 7); FPD (Tube, Feeding, 1).
Next steps
- See all 8 Moss Medical Products clearances with predicates and recalls
- Run predicate analysis for product code KNT, Moss Medical Products'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.