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Acmi Corporation

United StatesFDA applicant, unverified

Devices
16
FDA recalls
4

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

Catalogue16

Newest first, rows 1-16 of 16

Search and filter all 16 devices
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Rows 1-16 of 16

FDA recalls4

Recalls are matched to the firm by name. FDA recall data as of 1 Nov 2026.

  • 2004

    • 30 Apr 2004 Z-0925-04 Unclassified (pre-2012) Terminated Product sterility may be compromised due to the lack of package seal integrity Distribution: Nationwide Foreign: Canada, Australa, Brazil, Korea, Mexico, Turkey Submission number: K980492
    • 30 Apr 2004 Z-0926-04 Unclassified (pre-2012) Terminated Product sterility may be compromised due to the lack of package seal integrity Distribution: Nationwide Foreign: Canada, Australa, Brazil, Korea, Mexico, Turkey Submission number: K980492
    • 30 Apr 2004 Z-0927-04 Unclassified (pre-2012) Terminated Product sterility may be compromised due to the lack of package seal integrity Distribution: Nationwide Foreign: Canada, Australa, Brazil, Korea, Mexico, Turkey Submission number: K980492
    • 30 Apr 2004 Z-0928-04 Unclassified (pre-2012) Terminated Product sterility may be compromised due to the lack of package seal integrity Distribution: Nationwide Foreign: Canada, Australa, Brazil, Korea, Mexico, Turkey Submission number: K980492

Frequently asked questions

How many devices does Acmi Corporation have in the registry?

The registry currently lists 16 devices for Acmi Corporation. Devices recorded under merged duplicate company entries are counted once.

Which registries list Acmi Corporation's devices?

Among its 16 most recently registered devices, Acmi Corporation has devices listed in FDA 510(k) (16 devices).

What risk classes do Acmi Corporation's devices fall under?

Among its 16 most recently registered devices, the classes recorded for Acmi Corporation's devices are Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for Acmi Corporation?

FDA recall records list 4 recalls initiated by Acmi Corporation, the most recent initiated on 30 Apr 2004. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from Acmi Corporation in the registry?

The most recently registered devices listed for Acmi Corporation include DUAL LUMEN CATHETER, BERKELEY V-10 VACUUM CURETTAGE SYSTEM, UROPASS URETERAL ACCESS SHEATH, MODEL 61224 and USA SERIES DUR 8 ELITE, USA SERIES DUR 8, MODELS DUR 8E, DUR 8.

Generated automatically from registry data and not verified by a human reviewer.