FDA applicant

Performance Instruments Corp.

Newburyport, MA1 decision1987–19870 recalls

FDA records 1 decision for Performance Instruments Corp. (Newburyport, MA) in 1987: 1 510(k) clearance. All are in product code FRG (Wrap, Sterilization). 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 hospital panel, where it files most

How often FDA has decided Performance Instruments Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Performance Instruments Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Performance”

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

Performance Surgical Instruments Corp. 2 Performance Medical, Inc. 1 Performance Plus, Inc. 1 Performance, Inc. 1 Performance Hyperbarics 1 Performance Water Systems, LLC 1 Performance Ent. 1

Performance Instruments Corp.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Performance”