Florida Probe
510(k) K875076
Florida Probe is a medical device (FDA Class I; FDA product code EIX, Probe, Periodontic) made by Florida Probe Corp., cleared under FDA 510(k) K875076 on 10 Mar 1988, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK875076 | Date10 Mar 1988 | StatusActive |
Official records
- FDA 510(k) database K875076
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- EIX
- Device class
- Class I
- Regulation
- 21 CFR Part 872.4565
- Advisory committee
- Dental
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code EIX (Probe, Periodontic).
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- Premier Probes 1004918 by PREMIER DENTAL PRODUCTS COMPANY
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- PROBE TIP/PERI PROBE/PERI PROBE COMP. by Pd International AB
- ACCUDENT ACCUPROBE by Accudent, Inc.
- ACCUTEK PERIODONTAL PROBE by Sweet Micro Systems, Inc.
- THE VIVACARE T.P.S. PROBE by Rms Div.
- ALBUMIN REAGENT by Alpkem Corp.
- DENTAL INSTRUMENTS - PROBES by Miltex, Inc.
- DISPOSABLE PERIODONTAL PROBE by Periodontal Health Brush, Inc.