Medical Device Manufacturer · US , Mchenry , IL

Hoyt Laboratories - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 1977

Total

Cleared

Denied

Hoyt Laboratories has 11 FDA 510(k) cleared dental devices. Based in Mchenry, US.

Historical record: 11 cleared submissions from 1977 to 1982.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

Hoyt Laboratories is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Hoyt Laboratories

11 devices

1-11 of 11

PREVI DENT PROPHYLAXIS MINT NDC

K780834 · EJR

Dental · 9d

Cleared Nov 09, 1977

REPLICA BONDING AGENT

K771881

Dental · 36d

Cleared Oct 20, 1977

REPLICA DENTAL COMPOSIT

K771880 · EBF

Dental · 16d

Cleared Oct 20, 1977

REPLICA DENTAL COMPOSITE-RADIOPAQUE

TOOTHBRUSH, PEDODONTIC, #0126-0188-00

K771183 · EFW

Dental · 16d

Cleared Jul 15, 1977

TOOTHBRUSH, ORTHODONTIC, #0126-0189-00

K771184 · EFW

Dental · 16d

Cleared Jul 15, 1977

PERIODONTIC TOOTHBRUSH, #0126-0190-00

K771185 · EFW

Dental · 16d

Hoyt Laboratories - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Hoyt Laboratories

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