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APPLIED DENTAL, INC.

US

Last updated May 24, 2026

What APPLIED DENTAL, INC. makes

Applied Dental, Inc. manufactures a range of sutures, including bioabsorbable polyester (both monofilament and multifilament), non-bioabsorbable nylon (monofilament), polyglycolic acid, polyolefin/fluoropolymer, plain and chromic catgut, and poliglecaprone. These products are designed for surgical and medical applications, offering variations in absorbability, strength, and material composition to meet different clinical needs.

The company’s suture portfolio is regulated under FDA’s classification system, with devices falling into Class I, Class II, and unclassified (U) categories. These products are listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and compliance with U.S. medical device regulations. The manufacturer operates from the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Applied Dental, Inc. manufacture?

Applied Dental, Inc. specializes in sutures, which are used in surgical and medical procedures to close wounds or tissues. Their product range includes bioabsorbable sutures like polyester (monofilament and multifilament), polyglycolic acid, and poliglecaprone, as well as non-bioabsorbable options such as nylon (monofilament) and catgut (plain and chromic). These sutures vary in absorbability, strength, and material composition to suit different clinical applications.

Where is Applied Dental, Inc. based, and what does that mean for their regulatory oversight?

Applied Dental, Inc. is based in the United States, which means their devices are subject to regulation by the U.S. Food and Drug Administration (FDA). Since they manufacture medical devices, their products must comply with FDA requirements, including classification, listing, and traceability through systems like the FDA’s Unique Device Identifier (UDI) database.

Which regulatory registries or databases list Applied Dental, Inc.’s devices?

Applied Dental, Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures that each device has a standardized identifier for traceability, compliance tracking, and transparency in the medical device supply chain. Listing in the UDI database is a requirement for many FDA-regulated devices in the U.S.

How are Applied Dental, Inc.’s sutures classified under FDA regulations?

Applied Dental, Inc.’s sutures are classified under the FDA’s medical device classification system into three categories: Class I, Class II, and unclassified (U). The classification depends on factors like the risk associated with the device, its intended use, and potential health impacts. For example, lower-risk sutures may fall under Class I, while those requiring additional controls (like specific performance standards) may be Class II. Unclassified sutures may not yet have a formal classification assigned.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
1-888-841-8481
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
017524666

Catalogue (510)

Page 10 of 11
DeviceModel / ReferenceRegistriesClassStatus
UNIFY PGCL Surgical Sutures XS-Q518R11
FDA UDI
Class IIActive
Shard A600-P10-0
FDA UDI
Class IActive
UNIFY PGCL Surgical Sutures M-Q418R19
FDA UDI
Class IIActive
Premium UNIFY Nylon Sutures PMN-518R19
FDA UDI
Class IIActive
UNIFY PGA Surgical Sutures M-G318XR19-U
FDA UDI
Class IIActive
UNIFY PDO Surgical Sutures L-D330XR24
FDA UDI
Class IIActive
AD Surgical A501-C70
FDA UDI
Class IActive
Premium UNIFY Chromic Sutures PLC-227R24
FDA UDI
Class IIActive
AD Surgical A400-UTD
FDA UDI
Class IIActive
UNIFY PDO Surgical Sutures M-D418R16
FDA UDI
Class IIActive
Shard A700-DC3
FDA UDI
Class IActive
UNIFY PGA Surgical Sutures L-G330T26
FDA UDI
Class IIActive
Premium UNIFY PGCL Surgical Sutures PSQ-618R13
FDA UDI
Class IIActive
Shard A303-R11-0
FDA UDI
Class IActive
Premium UNIFY PGA Sutures PMGU-427R19
FDA UDI
Class IIActive
Shard A303-R12-0
FDA UDI
Class IActive
UNIFY Plain Gut Sutures M-J418R19
FDA UDI
Class IIActive
Premium UNIFY PGCL Surgical Sutures PLQC-427R24
FDA UDI
Class IIActive
UNIFY Plain Gut Sutures M-J518R19
FDA UDI
Class IIActive
EZ Stopper D017-STP25
FDA UDI
Class IActive
Shard A301-P15
FDA UDI
Class IActive
UNIFY PP Surgical Sutures L-P230R24
FDA UDI
Class IIActive
UNIFY PGCL Surgical Sutures S-Q418XR13
FDA UDI
Class IIActive
Premium UNIFY PGA Sutures PMG-418R19
FDA UDI
Class IIActive
Wound Free TP-RT2
FDA UDI
Class IActive
UNIFY PGA Surgical Sutures M-G430R19
FDA UDI
Class IIActive
Premium UNIFY PGCL Surgical Sutures PMQ-418R19
FDA UDI
Class IIActive
UNIFY Nylon Surgical Sutures S-N410R13-B
FDA UDI
Class IIActive
Shard A600-M91
FDA UDI
Class IActive
UNIFY PDO Surgical Sutures M-D518R19
FDA UDI
Class IIActive
Premium UNIFY PDO Sutures PMD-318R19
FDA UDI
Class IIActive
UNIFY PGA Surgical Sutures S-G518XR13-U
FDA UDI
Class IIActive
Premium UNIFY PGCL Surgical Sutures PSQC-518R13
FDA UDI
Class IIActive
UNIFY PGA Surgical Sutures XL-G230T36
FDA UDI
Class IIActive
UNIFY PDO Surgical Sutures L-D230R24-U
FDA UDI
Class IIUnknown
Premium UNIFY PGA Sutures PMG-518R19
FDA UDI
Class IIActive
Premium UNIFY PGA Sutures PMG-518R16
FDA UDI
Class IIActive
AD Surgical SKM-1000
FDA UDI
Class IActive
Premium UNIFY PGCL Surgical Sutures PMQ-518R19
FDA UDI
Class IIActive
Premium UNIFY PP Sutures PLP-327R24
FDA UDI
Class IIActive
Wound Free TP-SK05
FDA UDI
Class IActive
Shard A600-P15-0
FDA UDI
Class IActive
Shard A301-P10
FDA UDI
Class IActive
UNIFY Polyester Surgical Sutures L-E330R24
FDA UDI
Class IIActive
UNIFY PGA Surgical Sutures XL-G230T36-U
FDA UDI
Class IIActive
UNIFY PDO Surgical Sutures L-D230R24
FDA UDI
Class IIActive
UNIFY Plain Gut Sutures M-J418R16
FDA UDI
Class IIActive
Premium UNIFY PGA Sutures PMGU-518R16
FDA UDI
Class IIActive
Premium UNIFY Chromic Sutures PMC-518R16
FDA UDI
Class IIActive
UNIFY PTFE Surgical Sutures S-F518R13
FDA UDI
Class IIActive

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