FDA applicant

Rhino Mfg.

Rancho Cordova, CA2 decisions1992–19930 recalls

FDA records 2 decisions for Rhino Mfg. (Rancho Cordova, CA) from 1992 to 1993: 2 510(k) clearances. All are in product code FQO (Table, Operating-Room, Ac-Powered). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided Rhino Mfg.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rhino Mfg. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Rhino Mfg. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Rhino”

FDA records each applicant name separately; these may or may not be the same firm.

Rhino Health, Inc. 3 Rhino Metrics A/S 2

Rhino Mfg.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Rhino”