S. Jackson, Inc.
Alexandria, VA, US
S. JACKSON, INC. appears in FDA device records in Alexandria, VA. FDA records list 16 510(k) clearances between and , 14 PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 16 510(k) clearances for S. Jackson, Inc. between 1980 and 2008. The busiest year on record is 1983, with 5. The most recent is 2008, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1980 | 1 |
| 1982 | 1 |
| 1983 | 5 |
| 1985 | 1 |
| 1990 | 1 |
| 1991 | 1 |
| 1992 | 1 |
| 1993 | 3 |
| 1997 | 1 |
| 2008 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K080216 | SUPRAMESH EXTRA | FTL | Substantially Equivalent | |
| K973379 | STERILE SUPRAFOIL SMOOTH NYLON FOIL SHEETS | FTM | Substantially Equivalent | |
| K931614 | MOPYLEN SUTURE | GAW | Substantially Equivalent | |
| K931613 | SUPRAMID SUTURE | GAR | Substantially Equivalent | |
| K931612 | NYLAMID SUTURE | GAR | Substantially Equivalent | |
| K922630 | MOPYLEN | GAW | Substantially Equivalent | |
| K912429 | N80-838 SUPRAMID EXTRA SUTURE | GAR | Substantially Equivalent | |
| K904052 | SUPRAMID EXTRA SUTURES | GAR | Substantially Equivalent | |
| K852011 | NYLAMID MESH PAD FULL & HALF | FTM | Substantially Equivalent | |
| K831725 | FOIL IN 3 FORMS-NON-STERILE SHEETS | FTM | Substantially Equivalent | |
| K831727 | QUARTER GLOBE CAPS | FTM | Substantially Equivalent | |
| K831724 | CHIN (MENTOPLASTY) IMPLANTS | FWP | Substantially Equivalent | |
| K831723 | SUPRAMID EXTRA SURGICAL MESH | FTM | Substantially Equivalent | |
| K831726 | EYE MUSCLE SLEEVES | FTM | Substantially Equivalent | |
| K813589 | SHARTPOINT EYED NEEDLES | GDL | Substantially Equivalent | |
| K802780 | JACKSON HYDRO SYSTEM | FNG | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 1111225 | 1111225 | S. JACKSON, INC. | 15 Roth St, ALEXANDRIA, VA 22314 US | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
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.
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.
MDM coverage
MDM coverage of this company lists here, newest first. Submit news.
Is this your company?
This page is built from public FDA records. Company pages are free and factual, and stay free whether or not anyone claims them. Membership never changes editorial coverage or vetting outcomes.
Claiming lets S. Jackson, Inc. edit what it says about itself and list the categories it works in. It grants no badge: claiming is not verification.
Data as of , FDA export datePage updated Source: openFDA, public domain