Exelint International, Co.
Exelint International, Co. appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Dec 12, 2025.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K251089 | EXEL Disposable Syringe; EXEL Disposable Syringe with Needle; EXEL Disposable Syringe with Secure To | Dec 12, 2025 |
| K152183 | EXELINT SecureTouch Safety Hypodermic Needle | Nov 2, 2015 |
| K101309 | EXELINT ALUMINUM HUB BLUNT NEEDLES | Oct 20, 2010 |
| K020189 | EXEL BUTTERFLY SCALP VEIN SET | Mar 27, 2003 |
| K010197 | EXEL SECURE TOUCH SAFETY (P.S.V.) SCALP VEIN SET | May 14, 2001 |
| K003627 | EXEL SECURE TOUCH SAFETY A.V. FISTULA NEEDLE SET | Feb 8, 2001 |
| K001496 | A.V. FISTULA NEEDLE | Aug 1, 2000 |