Valley Forge Scientific Corp.
Oaks, PA, US
Valley Forge Scientific Corp. appears in FDA device records in Oaks, PA. FDA records list 27 510(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
- 27
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 27 510(k) clearances for Valley Forge Scientific Corp. between 1980 and 2005. The busiest year on record is 1985, with 4. The most recent is 2005, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1980 | 1 |
| 1983 | 1 |
| 1985 | 4 |
| 1986 | 2 |
| 1987 | 1 |
| 1989 | 2 |
| 1990 | 1 |
| 1991 | 1 |
| 1992 | 1 |
| 1993 | 2 |
| 1995 | 2 |
| 1996 | 1 |
| 1997 | 3 |
| 1998 | 1 |
| 2003 | 1 |
| 2004 | 2 |
| 2005 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K050364 | MALIS 2000 BIPOLAR ELECTROSURGICAL SYSTEM | GEI | Substantially Equivalent | |
| K042604 | VALLY FORGE SCIENTIFIC MALIS BIPOLAR DISPOSABLE FINGER OPERATED ELECTROSURGICAL INSTRUMENTS | GEI | Substantially Equivalent | |
| K032601 | STRYKER INTERVENTIONAL PAIN RF GENERATOR | GXD | Substantially Equivalent | |
| K033499 | MALIS IRRIGATION MODULE 1000 | GEI | Substantially Equivalent | |
| K982229 | BI-DENT | EKZ | Substantially Equivalent | |
| K973554 | VALLEY FORGE BIPOLAR BALL TIP ELECTRODE | JOS | Substantially Equivalent | |
| K971986 | VALLEY FORGE BIPOLAR LOOP | HGI | Substantially Equivalent | |
| K964143 | MINI-SYMM BIPOLAR COAGULATOR | GEI | Substantially Equivalent | |
| K955764 | VALLEY FORGE BIPLOAR LOOP | GEI | Substantially Equivalent | |
| K955346 | VFS - 300 BIPOLAR ELECTROSURGERY SYSTEM | GEI | Substantially Equivalent | |
| K951985 | PRECISION BIPOLAR COAGULATOR | GEI | Substantially Equivalent | |
| K930429 | AID, CARDIOPULMONARY RESUSCITATION | BTM | Substantially Equivalent | |
| K923928 | BIPOLAR COAGULATOR/IRRIAGATION SYSTEM | GEI | Substantially Equivalent | |
| K924188 | BI-TECH I BIPOLAR COAGULATOR/CUTTING SYSTEM | GEI | Substantially Equivalent | |
| K910510 | VALLEY FORGE BIPOLAR PEN OR FORCEPS | GEI | Substantially Equivalent | |
| K896541 | MALIS BIPOLAR ELECTROSURGICAL SYSTEM CMC-III | GEI | Substantially Equivalent | |
| K890648 | MALIS BIPOLAR CORD/IRRIGATION TUBING SET | GEI | Substantially Equivalent | |
| K890309 | MALIS SURGICAL STOOL | FZM | Substantially Equivalent | |
| K874845 | MALIS SURGICAL LOUPES | HJH | Substantially Equivalent | |
| K861822 | MALIS SURGICAL MESH FOR SKULL /SPINAL COLUMN REPAI | GWO | Substantially Equivalent | |
| K853992 | VALLEY FORGE SCIEN-TENS UNIT & ACCESS. LEAD WIRE & | GZJ | Substantially Equivalent | |
| K854592 | MALIS MICRO BIPOLAR COAGULATOR | GEI | Substantially Equivalent | |
| K854413 | MALIS IRRIGATION SYSTEM | GEI | Substantially Equivalent | |
| K852075 | SITE-MALIS BIPOLAR COAGULATOR MODULE | HQO | Substantially Equivalent | |
| K853168 | MALIS BIPOLAR PEN | GEI | Substantially Equivalent | |
| K831508 | MALIS CMC-II BIPOLAR COAGULATOR & CUT | GEI | Substantially Equivalent | |
| K801310 | THE MAGTEC SYSTEM | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- HGIElectrocautery, Gynecologic (And Accessories)
- JOSElectrode, Electrosurgical
- GEIElectrosurgical, Cutting & Coagulation & Accessories
- GXDGenerator, Lesion, Radiofrequency
- HJHLoupe, Binocular, Low Power
- GWOPlate, Cranioplasty, Preformed, Alterable
- GZJStimulator, Nerve, Transcutaneous, For Pain Relief
- FZMStool, Operating-Room
- HQOUnit, Cautery, Thermal, Ac-Powered
- EKZUnit, Electrosurgical, And Accessories, Dental
- BTMVentilator, Emergency, Manual (Resuscitator)
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