FDA applicant

Cypress Medical Mfg., Inc.

Palm Desert, CA2 decisions1989–19890 recalls

FDA records 2 decisions for Cypress Medical Mfg., Inc. (Palm Desert, CA) in 1989: 2 510(k) clearances. All are in product code HWC (Screw, Fixation, Bone). 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, orthopedic panel, where it files most

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

FDA decisions per year

No FDA decision for Cypress Medical Mfg., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Cypress”

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

Cypress Medical Products, Ltd. 26 Cypress Ent. 1

Cypress Medical Mfg., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Cypress”