Biomedics
Mchenry, IL, US
Biomedics appears in FDA device records in Mchenry, IL. FDA records list 10 510(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
- 10
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 10 510(k) clearances for Biomedics between 1980 and 1999. The busiest year on record is 1985, with 2. The most recent is 1999, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1980 | 1 |
| 1985 | 2 |
| 1995 | 2 |
| 1996 | 1 |
| 1997 | 1 |
| 1998 | 1 |
| 1999 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K992330 | THE BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY | JEY | Substantially Equivalent | |
| K984583 | THE BIOPLATE SHUNT CONNECTOR | JXG | Substantially Equivalent | |
| K980983 | THE BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY | JEY | Substantially Equivalent | |
| K972463 | THE BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY | JEY | Substantially Equivalent | |
| K961976 | THE BIOPLATE FIXATION SYSTEM | JEY | Substantially Equivalent | |
| K953273 | BIOPLATE RIGID FIXATION BONE PLATING SYSTEM | JEY | Substantially Equivalent | |
| K943071 | THE TITANIUM FIXATION SYSTEM | JEY | Substantially Equivalent | |
| K844787 | BIOMETRIC TOTAL HIP SYSTEM | JDI | Substantially Equivalent | |
| K842687 | BIOMEDICS BLADDER SCANNER | ITX | Substantially Equivalent | |
| K801345 | KAMPNER HINGED TOE PROSTHESIS | KWH | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain