Data / Medical devices / United States / TNT Moborg Intl. Ltd.
TNT Moborg Intl. Ltd.: FDA-registered device maker in Williamsville, NY, United States, 1 510(k) clearance
TNT Moborg Intl. Ltd. is registered with the FDA (registration 1319454) in Williamsville, NY, United States. It lists 5 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 14, 1994. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1319454
- FEI number
- 1000120304
- Address
- 8171 Main ST, Williamsville, NY, United States, 14221
- Owner or operator
- TNT MOBORG INTL. LTD. (9002671)
- Roles
- Specification developer
- First device listed
- July 15, 1992
- Registered through
- 2026
- Brand names listed
- immobile D, immobile E, immobile F, immobile a, immobile b, immobile c
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Administration Set Securement Device | PUK | 1 | Specification developer | accessdata.fda.gov |
| Cotton, Roll | EFN | 1 | Specification developer | accessdata.fda.gov |
| Device, Intravascular Catheter Securement | KMK | 1 | Specification developer | accessdata.fda.gov |
| Tape And Bandage, Adhesive | KGX | 1 | Specification developer | accessdata.fda.gov |
| Tape And Bandage, Adhesive, Adjustable Closing Mechanism, Otc Use | PYO | 1 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| July 14, 1994 | K941940 | IMMOBILE STERILE AND IMMOBILE A/C STERILE | KMK | Substantially Equivalent | Tnt Moborg Intl. , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Cotton, Roll
- All makers of Tape And Bandage, Adhesive
- All makers of Administration Set Securement Device
- All makers of Device, Intravascular Catheter Securement
- All makers of Tape And Bandage, Adhesive, Adjustable Closing Mechanism, Otc Use
Updated July 14, 1994. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.