Data / Medical devices / United States / Beutlich Pharmaceuticals, LLC
Beutlich Pharmaceuticals, LLC: FDA-registered device maker in Bunnell, FL, United States, 1 510(k) clearance
Beutlich Pharmaceuticals, LLC is registered with the FDA (registration 1413399) in Bunnell, FL, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 23, 1998. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1413399
- Address
- 7775 S US Hwy 1 Unit H, Bunnell, FL, United States, 32110
- Owner or operator
- BEUTLICH PHARMACEUTICALS, LLC (9023834)
- Roles
- Repackager or relabeler, Specification developer
- First device listed
- December 12, 2007
- Registered through
- 2026
- Brand names listed
- HurriPAK Periodontal Irrigation Tip, HurriPAK Periodontal Refill Kit, HurriSeal, HurriView II ® Two-Tone Plaque Indicating Snap-n-Go Swabs, HurriView ® Plaque Indicating Snap-n-Go Swabs
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Agent, Tooth Bonding, Resin | KLE | 2 | Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Container, Liquid Medication, Graduated | KYW | 1 | Repackager or relabeler | accessdata.fda.gov |
| Plaque Disclosing Agent | QJC | 1 | Repackager or relabeler, 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 |
|---|---|---|---|---|---|---|
| March 23, 1998 | K973002 | HURRISEAL DENTIN DESENSITIZER | KLE | Substantially Equivalent | Cheng & Assoc., Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Plaque Disclosing Agent
- All makers of Container, Liquid Medication, Graduated
- All makers of Agent, Tooth Bonding, Resin
Updated March 23, 1998. 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.