Mdt Corp., Inc.
Rochester, NY, US
Mdt Corp., Inc. appears in FDA device records in Rochester, NY. FDA records list 16 510(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
- 16
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 16 510(k) clearances for Mdt Corp., Inc. between 1988 and 1996. The busiest year on record is 1991, with 5. The most recent is 1996, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1988 | 1 |
| 1989 | 1 |
| 1991 | 5 |
| 1992 | 1 |
| 1993 | 3 |
| 1994 | 4 |
| 1996 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K960777 | MDT UNISPORE AND SPOR-TEST BIOLOGICALINDICATOR | FRC | Substantially Equivalent | |
| K942485 | MDT UROLOGY TABLE | MMZ | Substantially Equivalent | |
| K942486 | IMAGE FULL POWER EXAMINATION/MINOR SURGERY TABLE | FQO | Substantially Equivalent | |
| K924380 | MDT/HARVEY MODEL 7000 & 8000 CHEMICLAVE | MLR | Substantially Equivalent | |
| K926081 | DENTAL LIGHT | EAZ | Substantially Equivalent | |
| K924955 | MDT/HARVEY MC-8 AND MC-10 | FLE | Substantially Equivalent | |
| K931169 | MDT DENTAL CHAIR | KLC | Substantially Equivalent | |
| K920930 | MDT/CASTLE 10/90 DUAL LOAD STATION | FLF | Substantially Equivalent | |
| K922212 | MDT CASTLE BIOSIGN TEST PACK | FRC | Substantially Equivalent | |
| K914758 | MDT/SHAMPAINE MODEL 4900B SURGICAL TABLE | GDC | Substantially Equivalent | |
| K915393 | MDT/SHAMPAINE MODEL 4900E SURGICAL TABLE | GDC | Substantially Equivalent | |
| K914697 | MDT/CASTLE PURUS DENTAL UNIT | EIA | Substantially Equivalent | |
| K914076 | MDT/CASTLE 2000 SURGICAL LIGHTS | FSY | Substantially Equivalent | |
| K910663 | BOVIE MODEL X-10, X-10I, ELECTROSURGICAL GENERATOR | GEI | Substantially Equivalent | |
| K891366 | BIOSIGN BIOLOGICAL INDICATOR (EIGHT MONTH EXP.) | FRC | Substantially Equivalent | |
| K882713 | REBUILDING STERILIZERS | FLE | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- KLCChair, Dental, With Operative Unit
- GEIElectrosurgical, Cutting & Coagulation & Accessories
- FRCIndicator, Biological Sterilization Process
- EAZLight, Operating, Dental
- FSYLight, Surgical, Ceiling Mounted
- MLRSterilizer, Chemical
- FLFSterilizer, Ethylene-Oxide Gas
- FLESterilizer, Steam
- MMZTable, Cystometric, Electric
- FQOTable, Operating-Room, Ac-Powered
- GDCTable, Operating-Room, Electrical
- EIAUnit, Operative Dental
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