Data / Medical devices / United States / Pacon Manufacturing Company LLC
Pacon Manufacturing Company LLC: FDA-registered device maker in Navassa, NC, United States, 2 510(k) clearances
Pacon Manufacturing Company LLC is registered with the FDA (registration 3015709932) in Navassa, NC, United States. It lists 4 device types. The FDA files 2 510(k) clearances under its listings, the newest dated March 15, 1986. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3015709932
- Address
- 100 Quality Drive, Navassa, NC, United States, 28451
- Owner or operator
- Pacon Manufacturing Company LLC (10061163)
- Roles
- Contract manufacturer, Manufacturer, Repackager or relabeler
- First device listed
- September 3, 2019
- Registered through
- 2027
- Brand names listed
- Drape, Surgical, Dressing, Wound, hydrophilic, Fiber, Medical, Absorbent, Pacon Surgical Drapes
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Drape, Surgical, Antimicrobial | KKX | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Drape, Surgical, Exempt | PUI | 2 | Repackager or relabeler | accessdata.fda.gov |
| Dressing, Wound, Hydrophilic | NAC | 1 | Manufacturer | accessdata.fda.gov |
| Fiber, Medical, Absorbent | FRL | 1 | Contract manufacturer | 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 |
|---|---|---|---|---|---|---|
| March 15, 1986 | K850960 | NON-ABSORBENT DRAPES & ABSORBENT TOWELS | KKX | Substantially Equivalent | Excel Health Care Products | accessdata.fda.gov |
| February 21, 1985 | K850199 | POLY-LINED TOWEL/DRAPE LINE | KKX | Substantially Equivalent | Excel Health Care Products | accessdata.fda.gov |
Compare with other makers
- All makers of Drape, Surgical, Antimicrobial
- All makers of Fiber, Medical, Absorbent
- All makers of Dressing, Wound, Hydrophilic
- All makers of Drape, Surgical, Exempt
Updated March 15, 1986. 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.