Data / Medical devices / United States / Petoskey Plastics
Petoskey Plastics: FDA-registered device maker in Petoskey, MI, United States, 2 510(k) clearances
Petoskey Plastics is registered with the FDA (registration 3002696493) in Petoskey, MI, United States. It lists 4 device types. The FDA files 2 510(k) clearances under its listings, the newest dated January 30, 1997. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3002696493
- Address
- 4226 US 31 South, Petoskey, MI, United States, 49770
- Owner or operator
- Petoskey Plastics (10045287)
- Roles
- Manufacturer
- First device listed
- November 4, 2013
- Registered through
- 2026
- Brand names listed
- Dental Chair Cover non sterile
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Chair, Dental, Without Operative Unit | NRU | 1 | Manufacturer | accessdata.fda.gov |
| Container, Specimen, Non-Sterile | NNI | 1 | Manufacturer | accessdata.fda.gov |
| Cover, Barrier, Protective | MMP | 2 | Manufacturer | accessdata.fda.gov |
| Handpiece, Air-Powered, Dental | EFB | 1 | 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 |
|---|---|---|---|---|---|---|
| January 30, 1997 | K962288 | COVER-ALL, DRAPE-IT-ALL, CHAIR SLEVE, X-RAY SLEEVE, HEADREST COVER | MMP | Substantially Equivalent | Pinnacle Products, Inc. | accessdata.fda.gov |
| February 21, 1996 | K960352 | ALLRAP/SLIP-N-GRIP | EFB | Substantially Equivalent | Dental Disposables Intl., Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Container, Specimen, Non-Sterile
- All makers of Chair, Dental, Without Operative Unit
- All makers of Handpiece, Air-Powered, Dental
- All makers of Cover, Barrier, Protective
Updated January 30, 1997. 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.