FDA device listing
A SPECIFIC MEDICAL USE,Culture Plate,EQUIPMENT, LABORATORY,GENERAL PURPOSE,gongdong petri dish,Holder & Safety…
FDA device listing 1035499329 · Trademark Plastics Inc.
Key facts
| Proprietary names | A SPECIFIC MEDICAL USE,Culture Plate,EQUIPMENT, LABORATORY,GENERAL PURPOSE,gongdong petri dish,Holder & Safety Holder,Inoculation Loops,LABELED OR PROMOTED FOR,SPECIMEN COLLECTION HOLDER,Universal Tips ,Pipette tip with filter 10ul,20ul,100ul,200ul,1000ul,1250ul |
|---|---|
| Owner/operator | Trademark Plastics Inc. |
| Owner/operator number | 10087841 |
| Product codes | LXG |
| Device names | LXG - Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use |
| Device class | Class I |
| Classification regulations (21 CFR) | 862.2050 |
| Review panels | Clinical Chemistry |
| Registered establishments | TRADEMARK PLASTICS INC. |
| Establishment registrations | 3000682787 |
| FEI numbers | 3000682787 |
| Establishment operations | Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database