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Tulsa Dental Products LLC

United Statesfrom the FDA registration address FDA establishment FEI 1000554802

Tulsa Dental Products LLC is a medical device manufacturer, with 3,180 devices listed as of 12 Nov 2026.

Devices
3,180
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 12 Nov 2026

Registries
  • FDA GUDID 3,000

Among the 3,000 best-ranked of 3,180 devices.

Device classes
  • FDA Class I 2,941
  • FDA Class II 44
  • FDA Unclassified 15

Among the 3,000 best-ranked of 3,180 devices.

Identifiers
  • FDA FEI 1000554802

What Tulsa Dental Products LLC makes

The company manufactures single-use and reusable endodontic files and rasps for manual and rotary/reciprocating use, including nickel-titanium (NITI) instruments. It also produces synthetic gutta-percha, endodontic paper points, warm-bonded obturation systems, and single-use dental syringe needles. These products are designed for root canal treatment and related dental procedures.

The portfolio includes devices classified as Class I, Class II, and unclassified (U) under FDA regulations, all listed in the FDA’s Unique Device Identifier (UDI) database.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3,180

Newest first, rows 1-50 of 3,180

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Company details

FDA FEI number
1000554802
Address
608 ROLLING HILLS DRIVE, Johnson City, TN, 37604

Frequently asked questions

How many devices does TULSA DENTAL PRODUCTS LLC have in the registry?

The registry currently lists 3180 devices for TULSA DENTAL PRODUCTS LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list TULSA DENTAL PRODUCTS LLC's devices?

Among its 50 most recently registered devices, TULSA DENTAL PRODUCTS LLC has devices listed in FDA GUDID (50 devices).

What risk classes do TULSA DENTAL PRODUCTS LLC's devices fall under?

Among its 50 most recently registered devices, the classes recorded for TULSA DENTAL PRODUCTS LLC's devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from TULSA DENTAL PRODUCTS LLC in the registry?

The most recently registered devices listed for TULSA DENTAL PRODUCTS LLC include Endodontic Hand Instruments 668720, ProFile GT Rotary File GTR1202021, Endodontic Hand Instruments 6325008 and ProFile GT Rotary File GTR1004030.

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

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.