Fournitures Hospitalieres Industrie
Memphis, TN, US
Fournitures Hospitalieres Industrie appears in FDA device records in Memphis, TN. FDA records list 24 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 24
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 24 510(k) clearances for Fournitures Hospitalieres Industrie between 2002 and 2018. The busiest year on record is 2004, with 4. The most recent is 2018, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2002 | 1 |
| 2003 | 1 |
| 2004 | 4 |
| 2005 | 2 |
| 2006 | 1 |
| 2007 | 1 |
| 2008 | 1 |
| 2010 | 1 |
| 2011 | 1 |
| 2012 | 1 |
| 2013 | 1 |
| 2015 | 4 |
| 2017 | 4 |
| 2018 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K171789 | ARROW Reverse Porous Glenoid | PHX | Substantially Equivalent | |
| K163148 | BePOD® Foot Screws | HWC | Substantially Equivalent | |
| K163710 | BePOD® EZ Weil Screws | HWC | Substantially Equivalent | |
| K162068 | ARROW Anatomical Porous glenoid | MBF | Substantially Equivalent | |
| K170040 | BePOD Cannulated Arthrodesis Screws | HWC | Substantially Equivalent | |
| K150568 | ARROW Humeral stems size 6 and 16 | PHX | Substantially Equivalent | |
| K150471 | CalcaNail Orthopedic Arthrodesis Nail | HSB | Substantially Equivalent | |
| K150463 | CalcaNail Orthopedic Nail | HSB | Substantially Equivalent | |
| K142778 | ARROW Reverse Shoulder long keel and short keel glenoid base | PHX | Substantially Equivalent | |
| K120740 | COLS® FIXATION SYSTEM | MBI | Substantially Equivalent | |
| K112193 | ARROW REVERSE SHOULDER SYSTEM | PHX | Substantially Equivalent | |
| K113591 | COLS PEEK | HWC | Substantially Equivalent | |
| K093599 | ARROW ANATOMICAL SHOULDER SYSTEM | KWS | Substantially Equivalent | |
| K080974 | TLS FIXATION SYSTEM | HWC | Substantially Equivalent | |
| K070617 | CANNULATED SCREW | HWC | Substantially Equivalent | |
| K060367 | TENOLIG | GAT | Substantially Equivalent | |
| K052058 | MODIFICATION TO: TITANIUM TELEGRAPH HUMERAL NAIL | HSB | Substantially Equivalent | |
| K050556 | ALUMINA HEAD | LZO | Substantially Equivalent | |
| K042035 | ALUMINA HEAD | LZO | Substantially Equivalent | |
| K042332 | TITANIUM TELEGRAPH HUMERAL NAIL | HSB | Substantially Equivalent | |
| K041456 | SNAP-OFF SCREWS | HWC | Substantially Equivalent | |
| K031939 | BIO-EUROLIG INTERFERENCE SCREW | HWC | Substantially Equivalent | |
| K033510 | MODIFICATION TO TELEGRAPH HUMERAL NAIL | HSB | Substantially Equivalent | |
| K023241 | TELEGRAPH HUMERAL NAIL | HSB | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- MBIFastener, Fixation, Nondegradable, Soft Tissue
- LZOProsthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
- KWSProsthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
- MBFProsthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented
- HSBRod, Fixation, Intramedullary And Accessories
- HWCScrew, Fixation, Bone
- PHXShoulder Prosthesis, Reverse Configuration
- GATSuture, Nonabsorbable, Synthetic, Polyethylene
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain