Sil-Med Corp.
Mchenry, IL, US
Sil-Med Corp. appears in FDA device records in Mchenry, IL. FDA records list 29 510(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
- 29
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 29 510(k) clearances for Sil-Med Corp. between 1980 and 1997. The busiest year on record is 1985, with 5. The most recent is 1997, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1980 | 1 |
| 1981 | 3 |
| 1983 | 2 |
| 1984 | 3 |
| 1985 | 5 |
| 1986 | 1 |
| 1989 | 2 |
| 1991 | 1 |
| 1992 | 1 |
| 1994 | 2 |
| 1995 | 1 |
| 1996 | 5 |
| 1997 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K972521 | NAVIGATOR (STYLET) 2006 | GAH | Substantially Equivalent | |
| K961392 | ANTIMICROBIAL PERITONEAL DIALYSIS COIL CATHETER WITH SPI-ARGENT II | FJS | Substantially Equivalent | |
| K961194 | ANTIMICROBIAL MEDIASTINAL SILICONE DRAIN | GBW | Substantially Equivalent | |
| K961295 | SAPPHIRE LINE FLAT DRAIN/KIT WITH SPI-ARGENT II W/OR W/OUT TROCAR | GBX | Substantially Equivalent | |
| K960099 | PENROSE DRAIN MODELS 6001 - 6007 | GCY | Substantially Equivalent | |
| K955463 | GRIP-A-BOOTS | LXZ | Substantially Equivalent | |
| K942709 | MEDIASTINAL SILICONE DRAINS | GBW | Substantially Equivalent for Some Indications | |
| K926496 | SIL-SLIP (COATED/REGULAR(NON-COATED)THORACIC DRAIN | GBX | Substantially Equivalent | |
| K926495 | SIL-SLIP ROUND WOUND DRAIN (COATED)/BLUE STRIPE | GBX | Substantially Equivalent | |
| K926408 | SIL-SLIP FLAT SUCTION DRAIN | GBX | Substantially Equivalent | |
| K921424 | SIL-MED FLAT SUCTION DRAIN | GBX | Substantially Equivalent | |
| K903989 | SIL-MED T-TUBE DRAIN | HFL | Substantially Equivalent | |
| K891471 | SIL-MED WASTE FLUID DUMP BAG | KDG | Substantially Equivalent | |
| K885167 | TRUDELL BENT CATHETER | FJS | Substantially Equivalent | |
| K862767 | SILICONE SUMP DRAIN | GBS | Substantially Equivalent | |
| K854418 | ROUND SUCTION DRAIN | GBS | Substantially Equivalent | |
| K851195 | VASCULAR ACCESS CATHETER | LJS | Substantially Equivalent | |
| K851196 | INCISION DRAIN | GCD | Substantially Equivalent | |
| K851921 | Y CONNECTOR | GCD | Substantially Equivalent | |
| K850247 | PERITONEAL DIALYSIS COIL CATHETER | FXX | Substantially Equivalent | |
| K843575 | DERBYSHIRE DRAIN | GBW | Substantially Equivalent | |
| K842765 | SILIMED BREAST FORM | GBI | Substantially Equivalent | |
| K833872 | SAV-A-LIMB | KYR | Substantially Equivalent | |
| K830607 | SUCTION RESERVOIR | GCY | Substantially Equivalent | |
| K830610 | FLAT SUCTION DRAIN | GBC | Substantially Equivalent | |
| K813063 | FLAT DRAIN | GBW | Substantially Equivalent | |
| K813062 | VASCULAR PAWS | DXC | Substantially Equivalent | |
| K810080 | VASCULAR TIE (VAS-TIE) | KDC | Substantially Equivalent | |
| K801818 | TENCKHOFF CATHETER | FJS | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- GCYApparatus, Suction, Single Patient Use, Portable, Nonpowered
- KYRBag, Ice
- LJSCatheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
- GBXCatheter, Irrigation
- GBWCatheter, Peritoneal
- FJSCatheter, Peritoneal, Long-Term Indwelling
- GBSCatheter, Ventricular, General & Plastic Surgery
- KDGChisel (Osteotome)
- DXCClamp, Vascular
- GCDConnector, Catheter
- HFLDrain, Cervical
- LXZGuard, Instrument
- KDCInstrument, Surgical, Disposable
- GBCLamp, Surgical, Incandescent
- FXXMask, Surgical
- GBIMaterial, External Aesthetic Restoration, Used With Adhesive
- GAHStylet, Surgical, General & Plastic Surgery
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.
Where there is a record, this is where it appears: what was checked, when it was checked, and the current status. An MDM Verified badge on another website links to a verify address on this domain that resolves to this section. A badge that does not resolve here is not ours.
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Data as of , FDA export datePage updated Source: openFDA, public domain
