Medical Device Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 46
- FDA recalls
- 50
At a glance
Market reach
- United States
- FDA recalls
What Medical Device Technologies, Inc. makes
Medical Device Technologies, Inc. manufactures a range of medical devices including biliary drainage catheters, drainage catheter guidewires, and various biopsy needles such as aspiration, manual, and bone marrow biopsy sets. The company also produces specialized equipment including cell recovery systems, prostate stabilization and seeding kits, and needle-based localization devices like the Kopan's target.
The company is based in the United States and maintains a portfolio of products classified as Class I, Class II, and U. These devices are documented within the FDA 510(k) regulatory registry.
Catalogue
Search and filter all 46 devicesFDA recalls
FDA recall records list 50 recalls initiated by Medical Device Technologies, Inc., the earliest on 2004-03-02 and the most recent on 2010-12-22. By recorded status: 50 terminated. The reasons filed fall into these groups: sterility or contamination, packaging and mechanical integrity. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
2010
- 22 Dec 2010 Z-0214-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
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- 22 Dec 2010 Z-0215-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
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- 22 Dec 2010 Z-0216-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
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- 22 Dec 2010 Z-0217-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
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- 22 Dec 2010 Z-0218-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
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- 22 Dec 2010 Z-0219-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
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- 22 Dec 2010 Z-0220-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
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- 22 Dec 2010 Z-0221-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
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- 22 Dec 2010 Z-0222-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
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- 22 Dec 2010 Z-0223-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
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- 22 Dec 2010 Z-0214-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
Show the 25 most recent of 50 recalls
2010
- 22 Dec 2010 Z-0224-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
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- 22 Dec 2010 Z-0225-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
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- 22 Dec 2010 Z-0226-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
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- 22 Dec 2010 Z-0227-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
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- 22 Dec 2010 Z-0228-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
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- 22 Dec 2010 Z-0229-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
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- 22 Dec 2010 Z-0230-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
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- 22 Dec 2010 Z-0231-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
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- 22 Dec 2010 Z-0232-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
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- 22 Dec 2010 Z-0233-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
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- 22 Dec 2010 Z-0234-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
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- 22 Dec 2010 Z-0235-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
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- 22 Dec 2010 Z-0236-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
Full distribution text
- 22 Dec 2010 Z-0237-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
Full distribution text
- 22 Dec 2010 Z-0238-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
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- 22 Dec 2010 Z-0224-2012 Unclassified (pre-2012) Terminated Medical Device Technologies, Inc. dba Angiotech, is recalling HSG Procedure Trays and Bone Biopsy Trays distributed between December 2007 and December 14, 2010 for package integrity.
Frequently asked questions
How many devices does Medical Device Technologies, Inc. have in the registry?
The registry currently lists 46 devices for Medical Device Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medical Device Technologies, Inc.'s devices?
Among its 46 most recently registered devices, Medical Device Technologies, Inc. has devices listed in FDA 510(k) (46 devices).
What risk classes do Medical Device Technologies, Inc.'s devices fall under?
Among its 46 most recently registered devices, the classes recorded for Medical Device Technologies, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Medical Device Technologies, Inc.?
FDA recall records list 50 recalls initiated by Medical Device Technologies, Inc., the most recent initiated on 22 Dec 2010. 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 Medical Device Technologies, Inc. in the registry?
The most recently registered devices listed for Medical Device Technologies, Inc. include MANAN BILIARY DRAINAGE CATHETER, MANAN D BAG, ULTRA-CORE BIOPSY NEEDLES and MANAN TECHNA-CUT ASPIRATION NEEDLE.