Data / Medical devices / United States / Sterling Contract Packaging, Inc.
Sterling Contract Packaging, Inc.: FDA-registered device maker in Moore, SC, United States, 1 PMA approval
Sterling Contract Packaging, Inc. is registered with the FDA (registration 3008789244) in Moore, SC, United States. It lists 3 device types. The FDA files 1 PMA approval under its listings, the newest dated March 16, 1984. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008789244
- Address
- 1875 Moore-Duncan Hwy., Moore, SC, United States, 29369
- Owner or operator
- Sterling Contract Packaging, Inc. (10033763)
- Roles
- Repackager or relabeler
- First device listed
- March 6, 2020
- Registered through
- 2026
- Brand names listed
- Accessories, Soft Lens Products, KAZ/Helen of Troy, cara; kaz
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Soft Lens Products | LPN | 2 | Repackager or relabeler | accessdata.fda.gov |
| Humidifier, Non-Direct Patient Interface (Home-Use) | KFZ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Pad, Heating, Powered | IRT | 2 | Repackager or relabeler | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| March 16, 1984 | P820069 | BOSTON LENS(R) CLEANER | LPN | 12 | August 15, 1994 | accessdata.fda.gov |
Compare with other makers
- All makers of Accessories, Soft Lens Products
- All makers of Humidifier, Non-Direct Patient Interface (Home-Use)
- All makers of Pad, Heating, Powered
Updated August 15, 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.