Joint Medical Products Corp.: FDA filings under this applicant name
FDA lists 33 510(k) clearances under the applicant name “Joint Medical Products Corp.” (first 1984, latest 1996), across 13 product codes in 1 review panel. Median 510(k) review time under this name: 147 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 |
|---|---|---|---|
| JDI | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented | 8 | 8 |
| JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 7 | 7 |
| LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented | 6 | 6 |
| LWJ | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented | 2 | 2 |
| HSX | Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer | 1 | 1 |
| JDG | Prosthesis, Hip, Femoral Component, Cemented, Metal | 1 | 1 |
| JDK | Prosthesis, Hip, Cement Restrictor | 1 | 1 |
| JDL | Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component) | 1 | 1 |
| KRO | Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer | 1 | 1 |
| KWZ | Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer | 1 | 1 |
Plus 3 more product codes.
Review panels
- Orthopedic (31)
Most recent Joint Medical Products Corp. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K955511 | ARTHOPOR I & II ACETABULAR CUP/ARTHOPOR II OBLONG ACETABULAR CUP | LPH | 1996-02-26 | 84 |
| K954935 | S-ROM FEMORAL HIP STEM - SIZE 14 X 8 | LPH | 1996-01-22 | 87 |
| K944321 | S-ROM NOILES POSTERIOR STABILIZED TOTAL KNEE SYSTEM II | JWH | 1995-08-14 | 346 |
| K951726 | S-ROM ZTP UHMWPE ACETABULAR CUP | JDI | 1995-06-21 | 68 |
| K951084 | S-ROM OPC (ONE-PIECE CEMENTED) II FEMORAL HIP PROSTHESIS | JDI | 1995-05-31 | 83 |
| K951000 | ZTT I AND II ACETABULAR CUP OF THE S-ROM TOTAL HIP SYSTEM | LPH | 1995-04-14 | 42 |
| K941769 | KNEE PROTHESIS | JWH | 1995-02-01 | 296 |
| K936037 | S-ROM NOILES CRUCIATE RETAINING KNEE | JWH | 1994-10-03 | 287 |
| K934412 | COATED ZT PROXIMAL SLEEVE | LPH | 1994-06-03 | 266 |
| K931676 | S-ROM(R) ZTT(TM) ACETABULAR CUP-APICAL HOLE PLUG | JDL | 1994-05-18 | 407 |
23 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Joint Medical Products Corp..
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.
- Joint Mobilizer Systems, Inc. (2 510(k)s)
- Joint Preservation Innovations, LLC (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Joint Medical Products Corp.?
FDA lists 33 510(k) clearances under the applicant name “Joint Medical Products Corp.” (first 1984, latest 1996), across 13 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 Joint Medical Products Corp.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Joint Medical Products Corp. is 147 days.
Which FDA product codes appear under Joint Medical Products Corp.?
The most frequent FDA product codes under this applicant name are JDI (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented, 8); JWH (Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer, 7); LPH (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented, 6).
Next steps
- See all 33 Joint Medical Products Corp. clearances with predicates and recalls
- Run predicate analysis for product code JDI, Joint Medical Products Corp.'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.